Главная http://orgchemlab.com/2-uncategorised.feed 2023-03-14T17:37:29+00:00 Joomla! - Open Source Content Management О проекте 2013-09-14T17:35:38+00:00 2013-09-14T17:35:38+00:00 http://orgchemlab.com/about-project.html Administrator ovmaltsev@gmail.com <div class="feed-description"><h1 align="center">О проекте</h1> <p>Сайт посвящен экспериментальной органической химии, в первую очередь, техникам работы с органическими веществами и методам анализа органических веществ.</p> <p><strong>Что меня заставило создать подобный проект?</strong></p> <ol> <li> <div align="justify"><strong>Передача опыта.</strong> Несмотря на высокий уровень образования в нашей стране выпускники-химики, да и просто студенты-дипломники часто теряются, когда остаются один на один с экспериментальной органической химией. Оказывается, что даже неукоснительное следование методикам проведения синтеза зачастую не приводит к высоким выходам продуктов реакций, сказывается отсутствие опыта.</div> </li> <li> <div align="justify"><strong>Отсутствие подобных проектов.</strong> На зарубежных сайтах образованию, в том числе химическому, посвящено большое множество ресурсов, однако, на русскоязычной стороне интернета подобных проектов немного.</div> </li> <li> <div align="justify"><strong>Дверь в мир экспериментальной органической химии</strong>. Для многих остается загадкой – чем занимаются ученые в своих лабораториях. Из чего складывается их работа. Совокупность данных на сайте приподнимет завесу тайны…</div> </li> </ol> <p align="justify">Смею надеяться, что ресурс привлечет и других энтузиастов, готовых поделиться экспериментальным опытом. Если у вас есть предложения о том, как можно улучшить проект, готовые тематические статьи (или идеи статей), а также предложения о сотрудничестве, вы можете присылать их на мой электронный ящик: ovmaltsev@gmail.com.</p> <p align="right">C Уважением,<br /><a href="index.php?option=com_content&amp;view=article&amp;id=72&amp;Itemid=196" title="Перейти на страницу автора">к.х.н. Мальцев О.В.</a>,<br />РХТУ им. Д.И.Менделеева</p></div> <div class="feed-description"><h1 align="center">О проекте</h1> <p>Сайт посвящен экспериментальной органической химии, в первую очередь, техникам работы с органическими веществами и методам анализа органических веществ.</p> <p><strong>Что меня заставило создать подобный проект?</strong></p> <ol> <li> <div align="justify"><strong>Передача опыта.</strong> Несмотря на высокий уровень образования в нашей стране выпускники-химики, да и просто студенты-дипломники часто теряются, когда остаются один на один с экспериментальной органической химией. Оказывается, что даже неукоснительное следование методикам проведения синтеза зачастую не приводит к высоким выходам продуктов реакций, сказывается отсутствие опыта.</div> </li> <li> <div align="justify"><strong>Отсутствие подобных проектов.</strong> На зарубежных сайтах образованию, в том числе химическому, посвящено большое множество ресурсов, однако, на русскоязычной стороне интернета подобных проектов немного.</div> </li> <li> <div align="justify"><strong>Дверь в мир экспериментальной органической химии</strong>. Для многих остается загадкой – чем занимаются ученые в своих лабораториях. Из чего складывается их работа. Совокупность данных на сайте приподнимет завесу тайны…</div> </li> </ol> <p align="justify">Смею надеяться, что ресурс привлечет и других энтузиастов, готовых поделиться экспериментальным опытом. Если у вас есть предложения о том, как можно улучшить проект, готовые тематические статьи (или идеи статей), а также предложения о сотрудничестве, вы можете присылать их на мой электронный ящик: ovmaltsev@gmail.com.</p> <p align="right">C Уважением,<br /><a href="index.php?option=com_content&amp;view=article&amp;id=72&amp;Itemid=196" title="Перейти на страницу автора">к.х.н. Мальцев О.В.</a>,<br />РХТУ им. Д.И.Менделеева</p></div> Страница автора 2013-09-14T19:07:54+00:00 2013-09-14T19:07:54+00:00 http://orgchemlab.com/oleg-maltsev-rus.html Administrator ovmaltsev@gmail.com <div class="feed-description"><div id="table_CV"> <div id="icon_table_CV"> <h1><a name="top1" title="top1"></a>Мальцев Олег (see <a href="index.php?option=com_content&amp;view=article&amp;id=112&amp;Itemid=197">English Version <img src="images/stories/English.jpg" border="0" height="20" align="absmiddle" /></a>)</h1> <div id="icon_table_CV"> <p><strong>E-mail для связи:</strong> contact[собака]orgchemlab.com</p> <a href="http://de.linkedin.com/pub/oleg-maltsev/88/a65/987"><span style="font: 80%/normal Arial, sans-serif; color: #0783b6; font-size-adjust: none; font-stretch: normal;"><img src="http://s.c.lnkd.licdn.com/scds/common/u/img/webpromo/btn_in_20x15.png" border="0" alt="См. профиль пользователя Oleg Maltsev в LinkedIn" width="20" height="15" align="absmiddle" /><span style="text-decoration: underline;"><span style="font-size: small;">Linkedin: см. профиль</span></span></span></a></div> <h1><span style="text-decoration: underline;"><span style="font-size: small;"><img src="../PractChemistry/images/stories/Author/Oleg_Maltsev_2.png" border="0" align="right" /></span></span></h1> <p> </p> <div id="icon_table_CV"> <h4 align="left">Образование ______________________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid" style="width: 70px;"> <p><strong>2006</strong></p> </td> <td class="mceVisualAid"> <p><strong><span style="font-family: Tahoma;">Бакалавр. </span></strong><span style="font-family: Tahoma;">Специализация</span><span style="font-family: Tahoma;">: Химическая технология и биотехнология.</span><br />Российский химико-технологический Университет им. Д. И. Менделеева</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2008</strong></td> <td class="mceVisualAid"><strong>Инженер.</strong> <span style="font-family: Tahoma;">Специализация</span><span style="font-family: Tahoma;">: Химическая технология биологически активных веществ.</span><br />Российский химико-технологический Университет им. Д. И. Менделеева</td> </tr> <tr> <td class="mceVisualAid"><strong>2011</strong></td> <td class="mceVisualAid"><strong>Кандидат химических наук.</strong> <span style="font-family: Tahoma;">Специализация</span><span style="font-family: Tahoma;">: Органическая химия, Технология органических веществ. Р</span>оссийский химико-технологический Университет им. Д. И. Менделеева. <br />Институт органической химии им. Н.Д. Зелинского</td> </tr> </tbody> </table> <h4 align="left">Деятельность _____________________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid"><strong>2011 - н.в.</strong></td> <td class="mceVisualAid"><strong>Постдокторант.</strong> Лаборатория: "Каталитического Органического Синтеза"<br />Технологический Университет Мюнхена<br />Зав. лабораторией: проф. Лукас Хинтерманн</td> </tr> <tr> <td class="mceVisualAid" style="width: 70px;"><strong>2010 - н.в. </strong></td> <td class="mceVisualAid"> <p><strong>Ассистент.</strong> Кафедра: "Химии и технологии органического синтеза"<br /> Российский химико-технологический Университет им. Д. И. Менделеева<br />Зав. кафедрой: к.х.н. Попков С. В.</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2008 - <br />2012</strong></td> <td class="mceVisualAid"> <p><strong>Инженер-исследователь.</strong> Лаборатория: "Тонкого органического синтеза"<br /> Институт органической химии им. Н. Д. Зелинского РАН<br />Зав. лабораторией: д.х.н., проф. Злотин С. Г.</p> </td> </tr> <tr> <td class="mceVisualAid"> <p><strong>2007</strong></p> </td> <td class="mceVisualAid"> <p><strong>Летняя стажировка</strong><strong>.</strong> Лаборатория: "Общей Органической химии" <br />Институт органической химии Польской академии наук<br />Зав. лабораторией: проф. Макоша М.</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid"><strong>Летняя стажировка</strong><strong>.</strong> Лаборатория: "Общей Органической химии" <br />Институт органической химии Польской академии наук<br />Зав. лабораторией: проф. Макоша М.</td> </tr> <tr> <td class="mceVisualAid"><strong>2005 - 2008</strong></td> <td class="mceVisualAid"><strong>Инженер-исследователь.</strong> Лаборатория: "Синтеза биологически активных гетероциклических соединений"<br /> Институт элементоорганических соединений им. А. Н. Несмеянова РАН<br />Зав. лабораторией: д.х.н., проф. Вележева В. С.</td> </tr> <tr> <td class="mceVisualAid"><strong>2004 - 2005</strong></td> <td class="mceVisualAid"><strong>Стажер</strong><strong>.</strong> Лаборатория: "Химии карбенов и родственных интермедиатов" <br />Институт органической химии им. Н. Д. Зелинского РАН<br />Зав. лабораторией: акад. Егоров. М. П.</td> </tr> </tbody> </table> <h4 align="left">Награды и достижения ______________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid"><strong>2014</strong></td> <td class="mceVisualAid">Включен в биографический сборник Marquis’ “Who’s Who in the World” (31 издание 2014)</td> </tr> <tr> <td class="mceVisualAid"><strong>2012</strong></td> <td class="mceVisualAid">Награда за лучший стендовый доклад. ORCHEM, Ваймар, Германия</td> </tr> <tr> <td class="mceVisualAid"><strong>2012</strong></td> <td class="mceVisualAid">Медаль Российской академии наук с пре­мией для молодых ученых РАН в области общей и технической химии</td> </tr> <tr> <td class="mceVisualAid"><strong>2011</strong></td> <td class="mceVisualAid">Диплом кандидата химических наук</td> </tr> <tr> <td class="mceVisualAid"><strong>2010</strong></td> <td class="mceVisualAid">Лауреат (1 степени) конкурса работ<br />6 Конгресса молодых ученых по химии и химической технологии. <br />Секция: Химическая технология органических веществ и химико-фармацевтических средств</td> </tr> <tr> <td class="mceVisualAid"><strong>2008</strong></td> <td class="mceVisualAid">Диплом инженера с отличием</td> </tr> <tr> <td class="mceVisualAid"><strong>2007</strong></td> <td class="mceVisualAid">Лауреат (3 степени) конкурса молодых ученых (до 35 лет) <br />Института элементоорганических соединений им. А. Н. Несмеянова РАН</td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid">Лауреат конкурса студенческих научных работ <br />Института элементоорганических соединений им. А. Н. Несмеянова РАН</td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid">Диплом Бакалавра с отличием</td> </tr> <tr> <td class="mceVisualAid" style="width: 70px;"><strong>2002</strong> </td> <td class="mceVisualAid">Аттестат с отличием</td> </tr> </tbody> </table> <h4 align="left">Избранные публикации __________________</h4> <h4><strong>2014 </strong></h4> <p>1. O.V. Maltsev, N.K. Nath, P. Naumov, L. Hintermann. Why is Firefly Oxyluciferin a Notoriously Labile Substance? <em>Angew. Chem. Int. Ed.</em> <strong>2014</strong>, <em><span>53</span></em>, <span>847–850</span>. [<a href="http://dx.doi.org/10.1002/anie.201307972" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <h4><strong>2013 </strong></h4> <p>2. M.W. Jensen,  K. Støchkel, C. Kjær, J.L. Knudsen, Oleg V. Maltsev, L. Hintermann, P. Naumov, B.F. Milne, S.B. Nielsen. Photoinduced dissociation mass spectroscopy of firefly oxyluciferin anions. <em>Int. J. Mass Spectrom.</em> <strong>2013</strong>, DOI: 10.1016/j.ijms.2013.11.012. [<a href="http://dx.doi.org/10.1016/j.ijms.2013.11.012" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>3. O.V. Maltsev, V. Walter, M.J. Brandl, L. Hintermann. Medium Buffer Effects on the Condensation of L-Cysteine and Aryl Nitriles to (<em>R</em>)-2-Aryl-4,5-dihydrothiazole-4-carboxylic Acids. <em>Synthesis </em><strong>2013</strong>, <em>45</em>, 2763. [<a href="http://dx.doi.org/10.1055/s-0033-1339492" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p><a href="http://dx.doi.org/10.1039/C3SC90034G" target="_blank"><img src="../PractChemistry/images/stories/Author/Cover_2.jpg" border="0" width="100" align="right" /></a>4. M. Rebarz, B.-M. Kukovec, O.V. Maltsev, C. Ruckebusch, L. Hintermann, P. Naumov, M. Sliwa. Deciphering the Protonation and Tautomeric Equilibria of Firefly Oxyluciferin by Molecular Engineering and Multivariate Curve Resolution. <em>Chem. Sci.</em> <strong>2013</strong>, <span style="text-decoration: underline;">v.4</span>, 3803. [<a href="http://dx.doi.org/10.1039/C3SC50715G" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>5. K. Støchkel, C.N. Hansen, J. Houmøller, L.M. Nielsen, K. Anggara, M. Linares, P. Norman, F. Nogueira, O.V. Maltsev, L. Hintermann, S.B. Nielsen, P. Naumov, B.F. Milne. On the influence of water on the electronic structure of firefly oxyluciferin anions from absorption spectroscopy of bare and monohydrated ions in vacuo. <em>J. Am. Chem. Soc. </em><strong>2013</strong>, <span style="text-decoration: underline;">v.135</span>, 6485. [<a href="http://dx.doi.org/10.1021/ja311400t" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>6. L. Hintermann, M. Schmitz, O.V. Maltsev, P. Naumov. Organocatalytic Stereoisomerization versus Alkene Isomerization: Catalytic Asymmetric Synthesis of 1-Hydroxy-trans-2,5-diphenylphospholane 1-Oxide. <em>Synthesis </em><strong>2013</strong>, <span style="text-decoration: underline;">v.45</span>, 3, 308. [<a href="http://dx.doi.org/10.1055/s-0032-1316835" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>7. S.G. Zlotin, A.S. Kuherenko, O.V. Maltsev. A.O. Chizhov. Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts. <em>Top. Catal. </em><strong>2013</strong>, <span style="text-decoration: underline;">v.56</span>, 923. [<a href="http://dx.doi.org/10.1007/s11244-013-0056-8" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2012</h4> <p>8. A.S. Kucherenko, D.E. Siyutkin, O.V. Maltsev, S.V. Kochetkov, S.G. Zlotin. Asymmetric organocatalysis: from proline to highly efficient immobilized organocatalysts. <em>Russ. Chem. Bull.</em> <strong>2012</strong>, <span style="text-decoration: underline;">v.61</span>, 7, 1313. [<a href="http://dx.doi.org/10.1007/s11172-012-0177-4" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2011</h4> <p>9.O.V. Maltsev, I.P. Beletskaya, S.G. Zlotin. Organocatalytic Michael and Friedel–Crafts reactions in enantioselective synthesis of biologically active compounds. <em>Russ. Chem. Rev.</em> <strong>2011</strong>, <span style="text-decoration: underline;">v.80</span>, 11, 1067. [<a href="http://dx.doi.org/10.1070/RC2011v080n11ABEH004249" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p><a href="http://dx.doi.org/10.1002/chem.201190109" target="_blank"><img src="../PractChemistry/images/stories/Author/cover_1.gif" border="0" align="right" /></a>10. Maltsev, O.V.; Chizhov, A.O.; Zlotin, S.G. Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts: Deactivation Pathways of Jørgensen–Hayashi-type Catalysts in Asymmetric Michael Reactions. − <em>Chem. Eur. J.</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.17</span>, №22, 6109. [<a href="http://dx.doi.org/10.1002/chem.201100388" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>11. Maltsev, O.V.; Kucherenko, A.S., Zlotin, S.G. O-TMS-α,α-Diphenylprolinol derivatives supported on ionic polymers as recoverable organocatalysts for the asymmetric Michael reactions of carbon acids with α,β-enals. − <em>Mendeleev Commun.</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.21</span>, 146. [<a href="http://dx.doi.org/10.1016/j.mencom.2011.04.011" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2010</h4> <p>12. Maltsev, O.V.; Kucherenko, A.S.; Chimishkyan, A.L.; Zlotin, S.G. a,a-Diarylprolinol-derived Chiral Ionic Liquids − Recoverable Organocatalysts for the Domino Reaction between a,b-Enals and N-Protected Hydroxylamines. − <em>Tetrahedron: Asymmetry</em>, <strong>2010</strong>, <span style="text-decoration: underline;">v.21</span>, 2659 (Highlighted in <em>Synfacts</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.3</span>, 344 [<a href="http://dx.doi.org/10.1055/s-0030-1259461" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]). [<a href="http://dx.doi.org/10.1016/j.tetasy.2010.10.020" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>13. Maltsev, O.V.; Kucherenko, A.S.; Beletskaya, I.P.; Tartakovsky, V.A.; Zlotin, S.G. Chiral Ionic Liquids Bearing O-Silylated a,a-Diphenyl (S)- or (R)-Prolinol Units: Recoverable Organocatalysts for Asymmetric Michael Addition of Nitroalkanes to a,b-Enals. − <em>Eur. J. Org. Chem.</em>, <strong>2010</strong>, 2927. [<a href="http://dx.doi.org/10.1002/ejoc.201000239" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2009</h4> <p>14. Maltsev, O.V.; Kucherenko, A.S.; Zlotin, S.G. O-TMS-a,a-Diphenyl-(S)-prolinol Modified with an Ionic Liquid Moiety: A Recoverable Organocatalyst for the Asymmetric Michael Reaction between a,b-Enals and Dialkyl Malonates. − <em>Eur. J. Org. Chem.</em>, <strong>2009</strong>, 5134. [<a href="http://dx.doi.org/10.1002/ejoc.200900807" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2008</h4> <p>15. Mąkosza, M.; Sulikowski, D.; Maltsev, O.V. Enantioselective Synthesis of (R)-a-(p-Nitroaryl)prolines via Oxidative Nucleophilic Substitution of Hydrogen in Nitroarenes. - <em>Synlett.</em>, <strong>2008</strong>, <span style="text-decoration: underline;">v.11</span>, 1711. [<a href="http://dx.doi.org/10.1055/s-2008-1078483" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2007</h4> <p>16.  Mąkosza, M.; Surowiec, M.; Szczepańska, A.; Sulikowski, D.; Maltsev, O.V. Simple and General Synthesis of a-(p-Nitroaryl) Derivatives of Alanine and Serine. – <em>Synlett.</em>, <strong>2007</strong>, <span style="text-decoration: underline;">v.3</span>, 470. [<a href="http://dx.doi.org/10.1055/s-2007-967952" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>] </p> </div> </div> </div></div> <div class="feed-description"><div id="table_CV"> <div id="icon_table_CV"> <h1><a name="top1" title="top1"></a>Мальцев Олег (see <a href="index.php?option=com_content&amp;view=article&amp;id=112&amp;Itemid=197">English Version <img src="images/stories/English.jpg" border="0" height="20" align="absmiddle" /></a>)</h1> <div id="icon_table_CV"> <p><strong>E-mail для связи:</strong> contact[собака]orgchemlab.com</p> <a href="http://de.linkedin.com/pub/oleg-maltsev/88/a65/987"><span style="font: 80%/normal Arial, sans-serif; color: #0783b6; font-size-adjust: none; font-stretch: normal;"><img src="http://s.c.lnkd.licdn.com/scds/common/u/img/webpromo/btn_in_20x15.png" border="0" alt="См. профиль пользователя Oleg Maltsev в LinkedIn" width="20" height="15" align="absmiddle" /><span style="text-decoration: underline;"><span style="font-size: small;">Linkedin: см. профиль</span></span></span></a></div> <h1><span style="text-decoration: underline;"><span style="font-size: small;"><img src="../PractChemistry/images/stories/Author/Oleg_Maltsev_2.png" border="0" align="right" /></span></span></h1> <p> </p> <div id="icon_table_CV"> <h4 align="left">Образование ______________________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid" style="width: 70px;"> <p><strong>2006</strong></p> </td> <td class="mceVisualAid"> <p><strong><span style="font-family: Tahoma;">Бакалавр. </span></strong><span style="font-family: Tahoma;">Специализация</span><span style="font-family: Tahoma;">: Химическая технология и биотехнология.</span><br />Российский химико-технологический Университет им. Д. И. Менделеева</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2008</strong></td> <td class="mceVisualAid"><strong>Инженер.</strong> <span style="font-family: Tahoma;">Специализация</span><span style="font-family: Tahoma;">: Химическая технология биологически активных веществ.</span><br />Российский химико-технологический Университет им. Д. И. Менделеева</td> </tr> <tr> <td class="mceVisualAid"><strong>2011</strong></td> <td class="mceVisualAid"><strong>Кандидат химических наук.</strong> <span style="font-family: Tahoma;">Специализация</span><span style="font-family: Tahoma;">: Органическая химия, Технология органических веществ. Р</span>оссийский химико-технологический Университет им. Д. И. Менделеева. <br />Институт органической химии им. Н.Д. Зелинского</td> </tr> </tbody> </table> <h4 align="left">Деятельность _____________________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid"><strong>2011 - н.в.</strong></td> <td class="mceVisualAid"><strong>Постдокторант.</strong> Лаборатория: "Каталитического Органического Синтеза"<br />Технологический Университет Мюнхена<br />Зав. лабораторией: проф. Лукас Хинтерманн</td> </tr> <tr> <td class="mceVisualAid" style="width: 70px;"><strong>2010 - н.в. </strong></td> <td class="mceVisualAid"> <p><strong>Ассистент.</strong> Кафедра: "Химии и технологии органического синтеза"<br /> Российский химико-технологический Университет им. Д. И. Менделеева<br />Зав. кафедрой: к.х.н. Попков С. В.</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2008 - <br />2012</strong></td> <td class="mceVisualAid"> <p><strong>Инженер-исследователь.</strong> Лаборатория: "Тонкого органического синтеза"<br /> Институт органической химии им. Н. Д. Зелинского РАН<br />Зав. лабораторией: д.х.н., проф. Злотин С. Г.</p> </td> </tr> <tr> <td class="mceVisualAid"> <p><strong>2007</strong></p> </td> <td class="mceVisualAid"> <p><strong>Летняя стажировка</strong><strong>.</strong> Лаборатория: "Общей Органической химии" <br />Институт органической химии Польской академии наук<br />Зав. лабораторией: проф. Макоша М.</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid"><strong>Летняя стажировка</strong><strong>.</strong> Лаборатория: "Общей Органической химии" <br />Институт органической химии Польской академии наук<br />Зав. лабораторией: проф. Макоша М.</td> </tr> <tr> <td class="mceVisualAid"><strong>2005 - 2008</strong></td> <td class="mceVisualAid"><strong>Инженер-исследователь.</strong> Лаборатория: "Синтеза биологически активных гетероциклических соединений"<br /> Институт элементоорганических соединений им. А. Н. Несмеянова РАН<br />Зав. лабораторией: д.х.н., проф. Вележева В. С.</td> </tr> <tr> <td class="mceVisualAid"><strong>2004 - 2005</strong></td> <td class="mceVisualAid"><strong>Стажер</strong><strong>.</strong> Лаборатория: "Химии карбенов и родственных интермедиатов" <br />Институт органической химии им. Н. Д. Зелинского РАН<br />Зав. лабораторией: акад. Егоров. М. П.</td> </tr> </tbody> </table> <h4 align="left">Награды и достижения ______________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid"><strong>2014</strong></td> <td class="mceVisualAid">Включен в биографический сборник Marquis’ “Who’s Who in the World” (31 издание 2014)</td> </tr> <tr> <td class="mceVisualAid"><strong>2012</strong></td> <td class="mceVisualAid">Награда за лучший стендовый доклад. ORCHEM, Ваймар, Германия</td> </tr> <tr> <td class="mceVisualAid"><strong>2012</strong></td> <td class="mceVisualAid">Медаль Российской академии наук с пре­мией для молодых ученых РАН в области общей и технической химии</td> </tr> <tr> <td class="mceVisualAid"><strong>2011</strong></td> <td class="mceVisualAid">Диплом кандидата химических наук</td> </tr> <tr> <td class="mceVisualAid"><strong>2010</strong></td> <td class="mceVisualAid">Лауреат (1 степени) конкурса работ<br />6 Конгресса молодых ученых по химии и химической технологии. <br />Секция: Химическая технология органических веществ и химико-фармацевтических средств</td> </tr> <tr> <td class="mceVisualAid"><strong>2008</strong></td> <td class="mceVisualAid">Диплом инженера с отличием</td> </tr> <tr> <td class="mceVisualAid"><strong>2007</strong></td> <td class="mceVisualAid">Лауреат (3 степени) конкурса молодых ученых (до 35 лет) <br />Института элементоорганических соединений им. А. Н. Несмеянова РАН</td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid">Лауреат конкурса студенческих научных работ <br />Института элементоорганических соединений им. А. Н. Несмеянова РАН</td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid">Диплом Бакалавра с отличием</td> </tr> <tr> <td class="mceVisualAid" style="width: 70px;"><strong>2002</strong> </td> <td class="mceVisualAid">Аттестат с отличием</td> </tr> </tbody> </table> <h4 align="left">Избранные публикации __________________</h4> <h4><strong>2014 </strong></h4> <p>1. O.V. Maltsev, N.K. Nath, P. Naumov, L. Hintermann. Why is Firefly Oxyluciferin a Notoriously Labile Substance? <em>Angew. Chem. Int. Ed.</em> <strong>2014</strong>, <em><span>53</span></em>, <span>847–850</span>. [<a href="http://dx.doi.org/10.1002/anie.201307972" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <h4><strong>2013 </strong></h4> <p>2. M.W. Jensen,  K. Støchkel, C. Kjær, J.L. Knudsen, Oleg V. Maltsev, L. Hintermann, P. Naumov, B.F. Milne, S.B. Nielsen. Photoinduced dissociation mass spectroscopy of firefly oxyluciferin anions. <em>Int. J. Mass Spectrom.</em> <strong>2013</strong>, DOI: 10.1016/j.ijms.2013.11.012. [<a href="http://dx.doi.org/10.1016/j.ijms.2013.11.012" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>3. O.V. Maltsev, V. Walter, M.J. Brandl, L. Hintermann. Medium Buffer Effects on the Condensation of L-Cysteine and Aryl Nitriles to (<em>R</em>)-2-Aryl-4,5-dihydrothiazole-4-carboxylic Acids. <em>Synthesis </em><strong>2013</strong>, <em>45</em>, 2763. [<a href="http://dx.doi.org/10.1055/s-0033-1339492" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p><a href="http://dx.doi.org/10.1039/C3SC90034G" target="_blank"><img src="../PractChemistry/images/stories/Author/Cover_2.jpg" border="0" width="100" align="right" /></a>4. M. Rebarz, B.-M. Kukovec, O.V. Maltsev, C. Ruckebusch, L. Hintermann, P. Naumov, M. Sliwa. Deciphering the Protonation and Tautomeric Equilibria of Firefly Oxyluciferin by Molecular Engineering and Multivariate Curve Resolution. <em>Chem. Sci.</em> <strong>2013</strong>, <span style="text-decoration: underline;">v.4</span>, 3803. [<a href="http://dx.doi.org/10.1039/C3SC50715G" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>5. K. Støchkel, C.N. Hansen, J. Houmøller, L.M. Nielsen, K. Anggara, M. Linares, P. Norman, F. Nogueira, O.V. Maltsev, L. Hintermann, S.B. Nielsen, P. Naumov, B.F. Milne. On the influence of water on the electronic structure of firefly oxyluciferin anions from absorption spectroscopy of bare and monohydrated ions in vacuo. <em>J. Am. Chem. Soc. </em><strong>2013</strong>, <span style="text-decoration: underline;">v.135</span>, 6485. [<a href="http://dx.doi.org/10.1021/ja311400t" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>6. L. Hintermann, M. Schmitz, O.V. Maltsev, P. Naumov. Organocatalytic Stereoisomerization versus Alkene Isomerization: Catalytic Asymmetric Synthesis of 1-Hydroxy-trans-2,5-diphenylphospholane 1-Oxide. <em>Synthesis </em><strong>2013</strong>, <span style="text-decoration: underline;">v.45</span>, 3, 308. [<a href="http://dx.doi.org/10.1055/s-0032-1316835" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>7. S.G. Zlotin, A.S. Kuherenko, O.V. Maltsev. A.O. Chizhov. Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts. <em>Top. Catal. </em><strong>2013</strong>, <span style="text-decoration: underline;">v.56</span>, 923. [<a href="http://dx.doi.org/10.1007/s11244-013-0056-8" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2012</h4> <p>8. A.S. Kucherenko, D.E. Siyutkin, O.V. Maltsev, S.V. Kochetkov, S.G. Zlotin. Asymmetric organocatalysis: from proline to highly efficient immobilized organocatalysts. <em>Russ. Chem. Bull.</em> <strong>2012</strong>, <span style="text-decoration: underline;">v.61</span>, 7, 1313. [<a href="http://dx.doi.org/10.1007/s11172-012-0177-4" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2011</h4> <p>9.O.V. Maltsev, I.P. Beletskaya, S.G. Zlotin. Organocatalytic Michael and Friedel–Crafts reactions in enantioselective synthesis of biologically active compounds. <em>Russ. Chem. Rev.</em> <strong>2011</strong>, <span style="text-decoration: underline;">v.80</span>, 11, 1067. [<a href="http://dx.doi.org/10.1070/RC2011v080n11ABEH004249" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p><a href="http://dx.doi.org/10.1002/chem.201190109" target="_blank"><img src="../PractChemistry/images/stories/Author/cover_1.gif" border="0" align="right" /></a>10. Maltsev, O.V.; Chizhov, A.O.; Zlotin, S.G. Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts: Deactivation Pathways of Jørgensen–Hayashi-type Catalysts in Asymmetric Michael Reactions. − <em>Chem. Eur. J.</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.17</span>, №22, 6109. [<a href="http://dx.doi.org/10.1002/chem.201100388" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>11. Maltsev, O.V.; Kucherenko, A.S., Zlotin, S.G. O-TMS-α,α-Diphenylprolinol derivatives supported on ionic polymers as recoverable organocatalysts for the asymmetric Michael reactions of carbon acids with α,β-enals. − <em>Mendeleev Commun.</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.21</span>, 146. [<a href="http://dx.doi.org/10.1016/j.mencom.2011.04.011" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2010</h4> <p>12. Maltsev, O.V.; Kucherenko, A.S.; Chimishkyan, A.L.; Zlotin, S.G. a,a-Diarylprolinol-derived Chiral Ionic Liquids − Recoverable Organocatalysts for the Domino Reaction between a,b-Enals and N-Protected Hydroxylamines. − <em>Tetrahedron: Asymmetry</em>, <strong>2010</strong>, <span style="text-decoration: underline;">v.21</span>, 2659 (Highlighted in <em>Synfacts</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.3</span>, 344 [<a href="http://dx.doi.org/10.1055/s-0030-1259461" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]). [<a href="http://dx.doi.org/10.1016/j.tetasy.2010.10.020" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>13. Maltsev, O.V.; Kucherenko, A.S.; Beletskaya, I.P.; Tartakovsky, V.A.; Zlotin, S.G. Chiral Ionic Liquids Bearing O-Silylated a,a-Diphenyl (S)- or (R)-Prolinol Units: Recoverable Organocatalysts for Asymmetric Michael Addition of Nitroalkanes to a,b-Enals. − <em>Eur. J. Org. Chem.</em>, <strong>2010</strong>, 2927. [<a href="http://dx.doi.org/10.1002/ejoc.201000239" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2009</h4> <p>14. Maltsev, O.V.; Kucherenko, A.S.; Zlotin, S.G. O-TMS-a,a-Diphenyl-(S)-prolinol Modified with an Ionic Liquid Moiety: A Recoverable Organocatalyst for the Asymmetric Michael Reaction between a,b-Enals and Dialkyl Malonates. − <em>Eur. J. Org. Chem.</em>, <strong>2009</strong>, 5134. [<a href="http://dx.doi.org/10.1002/ejoc.200900807" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2008</h4> <p>15. Mąkosza, M.; Sulikowski, D.; Maltsev, O.V. Enantioselective Synthesis of (R)-a-(p-Nitroaryl)prolines via Oxidative Nucleophilic Substitution of Hydrogen in Nitroarenes. - <em>Synlett.</em>, <strong>2008</strong>, <span style="text-decoration: underline;">v.11</span>, 1711. [<a href="http://dx.doi.org/10.1055/s-2008-1078483" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2007</h4> <p>16.  Mąkosza, M.; Surowiec, M.; Szczepańska, A.; Sulikowski, D.; Maltsev, O.V. Simple and General Synthesis of a-(p-Nitroaryl) Derivatives of Alanine and Serine. – <em>Synlett.</em>, <strong>2007</strong>, <span style="text-decoration: underline;">v.3</span>, 470. [<a href="http://dx.doi.org/10.1055/s-2007-967952" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>] </p> </div> </div> </div></div> Информация об использовании материалов сайта 2013-09-14T19:08:45+00:00 2013-09-14T19:08:45+00:00 http://orgchemlab.com/copyrights.html Administrator ovmaltsev@gmail.com <div class="feed-description"><div id="icon"> <h2 align="center">Информация об использовании материалов сайта</h2> <p align="justify"><span style="font-family: Arial; font-size: small;"><img src="images/stories/attention.gif" border="0" align="left" />Перепубликация материалов данного сайта без письменного разрешения администратора сайта - <span style="color: #ff0000;"><strong>запрещена!</strong></span></span></p> <div> <ul> <li> <div align="justify"><span style="font-family: Arial; font-size: small;">Запрещается перепубликация материалов, размещённых на сайте. Перепубликация с наличием ссылки на оригинал на вашем сайте - не является оправданием и также запрещена. Любое использование размещенного на сайте материала требует письменного согласия автора!</span><span style="font-family: Arial; font-size: small;"><br /></span></div> </li> <li> <div align="justify"><span style="font-family: Arial; font-size: small;">Без разрешения, возможно только размещение коротких анонсов (до 300 знаков) со ссылкой на сайт с полной версией материала.</span></div> </li> </ul> </div> </div></div> <div class="feed-description"><div id="icon"> <h2 align="center">Информация об использовании материалов сайта</h2> <p align="justify"><span style="font-family: Arial; font-size: small;"><img src="images/stories/attention.gif" border="0" align="left" />Перепубликация материалов данного сайта без письменного разрешения администратора сайта - <span style="color: #ff0000;"><strong>запрещена!</strong></span></span></p> <div> <ul> <li> <div align="justify"><span style="font-family: Arial; font-size: small;">Запрещается перепубликация материалов, размещённых на сайте. Перепубликация с наличием ссылки на оригинал на вашем сайте - не является оправданием и также запрещена. Любое использование размещенного на сайте материала требует письменного согласия автора!</span><span style="font-family: Arial; font-size: small;"><br /></span></div> </li> <li> <div align="justify"><span style="font-family: Arial; font-size: small;">Без разрешения, возможно только размещение коротких анонсов (до 300 знаков) со ссылкой на сайт с полной версией материала.</span></div> </li> </ul> </div> </div></div> About author 2013-09-14T19:40:17+00:00 2013-09-14T19:40:17+00:00 http://orgchemlab.com/oleg-maltsev.html Administrator ovmaltsev@gmail.com <div class="feed-description"><div id="table_CV"> <div id="icon_table_CV"> <h1><a name="Top1" title="Top1"></a>Oleg Maltsev (см. <a href="index.php?option=com_content&amp;view=article&amp;id=72&amp;Itemid=196">Русскую Версию <img src="images/stories/Russian.jpg" border="0" height="25" align="absmiddle" /></a>)</h1> <div id="icon_table_CV"> <p><strong>Contact e-mail:</strong> contact[at]orgchemlab.com</p> <p><a href="http://de.linkedin.com/pub/oleg-maltsev/88/a65/987"><span style="font: 80%/normal Arial, sans-serif; color: #0783b6; font-size-adjust: none; font-stretch: normal;"><img src="http://s.c.lnkd.licdn.com/scds/common/u/img/webpromo/btn_in_20x15.png" border="0" alt="См. профиль пользователя Oleg Maltsev в LinkedIn" width="20" height="15" align="absmiddle" /><span style="text-decoration: underline;"><span style="font-size: small;">Linkedin: see profile.</span></span></span></a></p> </div> <h1><img src="../PractChemistry/images/stories/Author/Oleg_Maltsev_2.png" border="0" align="right" /></h1> <p> </p> <div id="icon_table_CV"> <h4>Education ______________________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid" style="width: 70px;"> <p><strong>2006</strong></p> </td> <td class="mceVisualAid"> <p><strong><span style="font-family: Tahoma;">Bachelor's degree. </span></strong><span style="font-family: Tahoma;">Specialization: Chemical Technology and Biotechnology.<br />D. I. Mendeleev University of Chemical Technology of Russia (Moscow, Russia).<br />Department of Technology of Organic Substances and Chemical Pharmaceutical Compounds.</span></p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2008</strong></td> <td class="mceVisualAid"><strong>M. Sc., Engineer.</strong> <span style="font-family: Tahoma;">Specialization: Chemical Technology of Synthetic Biologically Active Substances.<br />D. I. Mendeleev  University of Chemical Technology of Russia (Moscow, Russia).<br />Department of Technology of Organic Substances and Chemical Pharmaceutical Compounds.</span></td> </tr> <tr> <td class="mceVisualAid"><strong>2011</strong></td> <td class="mceVisualAid"><strong>Dr. degree. </strong><span style="font-family: Tahoma;">Specialization: Organic Chemistry. Technology of Organic Compounds. <br />N. D. Zelinsky Institute of Organic Chemistry RAS (Moscow, Russia) and <br />D. I. Mendeleev University of Chemical Technology of Russia (Moscow, Russia). </span></td> </tr> </tbody> </table> <h4>Experience _____________________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid"><strong>Since <br />2011</strong></td> <td class="mceVisualAid"><strong>PostDoc</strong><br /> Technische Universität München (München, Germany)<br />Laboratory of Catalytic Organic Synthesis<br />Head: Prof. Dr. Lukas Hintermann</td> </tr> <tr> <td class="mceVisualAid" style="width: 70px;"><strong>Since <br />2010  </strong></td> <td class="mceVisualAid"> <p><strong>Teaching Assistant</strong><br />D. I. Mendeleev University of Chemical Technology of Russia (Moscow, Russia)<br />Department of Technology of Organic Substances and Chemical Pharmaceutical Compounds. <br />Subdepartment of Chemistry and Technology of Organic Synthesis.<br />Head: Dr. S. V. Popkov</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2008-<br />2012 </strong></td> <td class="mceVisualAid"> <p><strong>Research Engineer, Junior Research Fellow<br /></strong>N. D. Zelinsky Institute of Organic Chemistry RAS (Moscow, Russia).<br />Laboratory of Fine Organic Synthesis. <br />Head: Prof. S. G. Zlotin</p> </td> </tr> <tr> <td class="mceVisualAid"> <p><strong>2007</strong></p> </td> <td class="mceVisualAid"> <p><strong>Summer Trainee <br /></strong>Institute of Organic Chemistry PAS (Warsaw, Poland). <br />Laboratory of General Organic Chemistry. <br />Head: Prof. M. Mąkosza</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid"><strong>Summer Trainee <br /> </strong>Institute of Organic Chemistry PAS (Warsaw, Poland). <br /> Laboratory of General Organic Chemistry. <br /> Head: Prof. M. Mąkosza</td> </tr> <tr> <td class="mceVisualAid"><strong>2005 - 2008</strong></td> <td class="mceVisualAid"><strong>Research Engineer <br /></strong>A. N. Nesmeyanov Institute of Elementorganic Compounds RAS (Moscow, Russia).<br />Laboratory of Synthesis of Heterocyclic Biological Active Substances. <br />Head: Prof. V. S. Velezheva</td> </tr> <tr> <td class="mceVisualAid"><strong>2004 - 2005</strong></td> <td class="mceVisualAid"><strong>Laboratory Assistant<br /></strong>N. D. Zelinsky Institute of Organic Chemistry RAS (Moscow, Russia). <br />Laboratory of Chemistry of Carbenes and Analogous Intermediates. <br />Head: Acad. M. P. Egorov</td> </tr> </tbody> </table> <h4>Awards ______________________</h4> <table class="mceVisualAid" width="738" border="0"> <tbody> <tr> <td class="mceVisualAid"><strong>2014</strong></td> <td class="mceVisualAid">Listed in the Marquis’ “Who’s Who in the World” Directory of Biographies (31st ed. 2014)</td> </tr> <tr> <td class="mceVisualAid"><strong>2012</strong></td> <td class="mceVisualAid">Best Poster Award. ORCHEM-2012</td> </tr> <tr> <td class="mceVisualAid"><strong>2012</strong></td> <td class="mceVisualAid">Prize of Russian Academy of Sciences for Junior Researchers in the field of General and Technical Chemistry</td> </tr> <tr> <td class="mceVisualAid"><strong>2011</strong></td> <td class="mceVisualAid">Doctor Degree</td> </tr> <tr> <td class="mceVisualAid"><strong>2010</strong></td> <td class="mceVisualAid">Laureate of “The 6th United Congress of Chemical Technology of Youth”</td> </tr> <tr> <td class="mceVisualAid"><strong>2008</strong></td> <td class="mceVisualAid">Master's Diploma: <em>magna cum laude</em></td> </tr> <tr> <td class="mceVisualAid"><strong>2007</strong></td> <td class="mceVisualAid"> <p>Laureate of “Competition of Young Scientists of A. N. Nesmeyanov<br />Institute of Elementorganic Compounds RAS” (up to 35 years)</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid">Laureate of “Conference of Student Research Works of <br />A.N. Nesmeyanov Institute of Elementorganic Compounds RAS"</td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid">Bachelor's Diploma: <em>magna cum laude </em></td> </tr> <tr> <td class="mceVisualAid" style="width: 70px;"><strong>2002</strong> </td> <td class="mceVisualAid">School leaving certificate: <em>magna cum laude </em></td> </tr> </tbody> </table> <h4 align="left">Selected Publications __________________</h4> <h4><strong>2014 </strong></h4> <p>1. O.V. Maltsev, N.K. Nath, P. Naumov, L. Hintermann. Why is Firefly Oxyluciferin a Notoriously Labile Substance? <em>Angew. Chem. Int. Ed.</em> <strong>2014</strong>, <em><span>53</span></em>, <span>847–850</span>. [<a href="http://dx.doi.org/10.1002/anie.201307972" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <h4><strong>2013 </strong></h4> <p>2. M.W. Jensen,  K. Støchkel, C. Kjær, J.L. Knudsen, Oleg V. Maltsev, L. Hintermann, P. Naumov, B.F. Milne, S.B. Nielsen. Photoinduced dissociation mass spectroscopy of firefly oxyluciferin anions. <em>Int. J. Mass Spectrom.</em> <strong>2013</strong>, DOI: 10.1016/j.ijms.2013.11.012. [<a href="http://dx.doi.org/10.1016/j.ijms.2013.11.012" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>3. O.V. Maltsev, V. Walter, M.J. Brandl, L. Hintermann. Medium Buffer Effects on the Condensation of L-Cysteine and Aryl Nitriles to (<em>R</em>)-2-Aryl-4,5-dihydrothiazole-4-carboxylic Acids. <em>Synthesis </em><strong>2013</strong>, <em>45</em>, 2763. [<a href="http://dx.doi.org/10.1055/s-0033-1339492" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p><a href="http://dx.doi.org/10.1039/C3SC90034G" target="_blank"><img src="../PractChemistry/images/stories/Author/Cover_2.jpg" border="0" width="100" align="right" /></a>4. M. Rebarz, B.-M. Kukovec, O.V. Maltsev, C. Ruckebusch, L. Hintermann, P. Naumov, M. Sliwa. Deciphering the Protonation and Tautomeric Equilibria of Firefly Oxyluciferin by Molecular Engineering and Multivariate Curve Resolution. <em>Chem. Sci.</em> <strong>2013</strong>, <span style="text-decoration: underline;">v.4</span>, 3803. [<a href="http://dx.doi.org/10.1039/C3SC50715G" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>5. K. Støchkel, C.N. Hansen, J. Houmøller, L.M. Nielsen, K. Anggara, M. Linares, P. Norman, F. Nogueira, O.V. Maltsev, L. Hintermann, S.B. Nielsen, P. Naumov, B.F. Milne. On the influence of water on the electronic structure of firefly oxyluciferin anions from absorption spectroscopy of bare and monohydrated ions in vacuo. <em>J. Am. Chem. Soc. </em><strong>2013</strong>, <span style="text-decoration: underline;">v.135</span>, 6485. [<a href="http://dx.doi.org/10.1021/ja311400t" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>6. L. Hintermann, M. Schmitz, O.V. Maltsev, P. Naumov. Organocatalytic Stereoisomerization versus Alkene Isomerization: Catalytic Asymmetric Synthesis of 1-Hydroxy-trans-2,5-diphenylphospholane 1-Oxide. <em>Synthesis </em><strong>2013</strong>, <span style="text-decoration: underline;">v.45</span>, 3, 308. [<a href="http://dx.doi.org/10.1055/s-0032-1316835" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>7. S.G. Zlotin, A.S. Kuherenko, O.V. Maltsev. A.O. Chizhov. Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts. <em>Top. Catal. </em><strong>2013</strong>, <span style="text-decoration: underline;">v.56</span>, 923. [<a href="http://dx.doi.org/10.1007/s11244-013-0056-8" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2012</h4> <p>8. A.S. Kucherenko, D.E. Siyutkin, O.V. Maltsev, S.V. Kochetkov, S.G. Zlotin. Asymmetric organocatalysis: from proline to highly efficient immobilized organocatalysts. <em>Russ. Chem. Bull.</em> <strong>2012</strong>, <span style="text-decoration: underline;">v.61</span>, 7, 1313. [<a href="http://dx.doi.org/10.1007/s11172-012-0177-4" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2011</h4> <p>9.O.V. Maltsev, I.P. Beletskaya, S.G. Zlotin. Organocatalytic Michael and Friedel–Crafts reactions in enantioselective synthesis of biologically active compounds. <em>Russ. Chem. Rev.</em> <strong>2011</strong>, <span style="text-decoration: underline;">v.80</span>, 11, 1067. [<a href="http://dx.doi.org/10.1070/RC2011v080n11ABEH004249" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p><a href="http://dx.doi.org/10.1002/chem.201190109" target="_blank"><img src="../PractChemistry/images/stories/Author/cover_1.gif" border="0" align="right" /></a>10. Maltsev, O.V.; Chizhov, A.O.; Zlotin, S.G. Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts: Deactivation Pathways of Jørgensen–Hayashi-type Catalysts in Asymmetric Michael Reactions. − <em>Chem. Eur. J.</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.17</span>, №22, 6109. [<a href="http://dx.doi.org/10.1002/chem.201100388" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>11. Maltsev, O.V.; Kucherenko, A.S., Zlotin, S.G. O-TMS-α,α-Diphenylprolinol derivatives supported on ionic polymers as recoverable organocatalysts for the asymmetric Michael reactions of carbon acids with α,β-enals. − <em>Mendeleev Commun.</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.21</span>, 146. [<a href="http://dx.doi.org/10.1016/j.mencom.2011.04.011" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2010</h4> <p>12. Maltsev, O.V.; Kucherenko, A.S.; Chimishkyan, A.L.; Zlotin, S.G. a,a-Diarylprolinol-derived Chiral Ionic Liquids − Recoverable Organocatalysts for the Domino Reaction between a,b-Enals and N-Protected Hydroxylamines. − <em>Tetrahedron: Asymmetry</em>, <strong>2010</strong>, <span style="text-decoration: underline;">v.21</span>, 2659 (Highlighted in <em>Synfacts</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.3</span>, 344 [<a href="http://dx.doi.org/10.1055/s-0030-1259461" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]). [<a href="http://dx.doi.org/10.1016/j.tetasy.2010.10.020" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>13. Maltsev, O.V.; Kucherenko, A.S.; Beletskaya, I.P.; Tartakovsky, V.A.; Zlotin, S.G. Chiral Ionic Liquids Bearing O-Silylated a,a-Diphenyl (S)- or (R)-Prolinol Units: Recoverable Organocatalysts for Asymmetric Michael Addition of Nitroalkanes to a,b-Enals. − <em>Eur. J. Org. Chem.</em>, <strong>2010</strong>, 2927. [<a href="http://dx.doi.org/10.1002/ejoc.201000239" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2009</h4> <p>14. Maltsev, O.V.; Kucherenko, A.S.; Zlotin, S.G. O-TMS-a,a-Diphenyl-(S)-prolinol Modified with an Ionic Liquid Moiety: A Recoverable Organocatalyst for the Asymmetric Michael Reaction between a,b-Enals and Dialkyl Malonates. − <em>Eur. J. Org. Chem.</em>, <strong>2009</strong>, 5134. [<a href="http://dx.doi.org/10.1002/ejoc.200900807" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2008</h4> <p>15. Mąkosza, M.; Sulikowski, D.; Maltsev, O.V. Enantioselective Synthesis of (R)-a-(p-Nitroaryl)prolines via Oxidative Nucleophilic Substitution of Hydrogen in Nitroarenes. - <em>Synlett.</em>, <strong>2008</strong>, <span style="text-decoration: underline;">v.11</span>, 1711. [<a href="http://dx.doi.org/10.1055/s-2008-1078483" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2007</h4> <p>16.  Mąkosza, M.; Surowiec, M.; Szczepańska, A.; Sulikowski, D.; Maltsev, O.V. Simple and General Synthesis of a-(p-Nitroaryl) Derivatives of Alanine and Serine. – <em>Synlett.</em>, <strong>2007</strong>, <span style="text-decoration: underline;">v.3</span>, 470. [<a href="http://dx.doi.org/10.1055/s-2007-967952" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>] </p> </div> </div> </div></div> <div class="feed-description"><div id="table_CV"> <div id="icon_table_CV"> <h1><a name="Top1" title="Top1"></a>Oleg Maltsev (см. <a href="index.php?option=com_content&amp;view=article&amp;id=72&amp;Itemid=196">Русскую Версию <img src="images/stories/Russian.jpg" border="0" height="25" align="absmiddle" /></a>)</h1> <div id="icon_table_CV"> <p><strong>Contact e-mail:</strong> contact[at]orgchemlab.com</p> <p><a href="http://de.linkedin.com/pub/oleg-maltsev/88/a65/987"><span style="font: 80%/normal Arial, sans-serif; color: #0783b6; font-size-adjust: none; font-stretch: normal;"><img src="http://s.c.lnkd.licdn.com/scds/common/u/img/webpromo/btn_in_20x15.png" border="0" alt="См. профиль пользователя Oleg Maltsev в LinkedIn" width="20" height="15" align="absmiddle" /><span style="text-decoration: underline;"><span style="font-size: small;">Linkedin: see profile.</span></span></span></a></p> </div> <h1><img src="../PractChemistry/images/stories/Author/Oleg_Maltsev_2.png" border="0" align="right" /></h1> <p> </p> <div id="icon_table_CV"> <h4>Education ______________________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid" style="width: 70px;"> <p><strong>2006</strong></p> </td> <td class="mceVisualAid"> <p><strong><span style="font-family: Tahoma;">Bachelor's degree. </span></strong><span style="font-family: Tahoma;">Specialization: Chemical Technology and Biotechnology.<br />D. I. Mendeleev University of Chemical Technology of Russia (Moscow, Russia).<br />Department of Technology of Organic Substances and Chemical Pharmaceutical Compounds.</span></p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2008</strong></td> <td class="mceVisualAid"><strong>M. Sc., Engineer.</strong> <span style="font-family: Tahoma;">Specialization: Chemical Technology of Synthetic Biologically Active Substances.<br />D. I. Mendeleev  University of Chemical Technology of Russia (Moscow, Russia).<br />Department of Technology of Organic Substances and Chemical Pharmaceutical Compounds.</span></td> </tr> <tr> <td class="mceVisualAid"><strong>2011</strong></td> <td class="mceVisualAid"><strong>Dr. degree. </strong><span style="font-family: Tahoma;">Specialization: Organic Chemistry. Technology of Organic Compounds. <br />N. D. Zelinsky Institute of Organic Chemistry RAS (Moscow, Russia) and <br />D. I. Mendeleev University of Chemical Technology of Russia (Moscow, Russia). </span></td> </tr> </tbody> </table> <h4>Experience _____________________________</h4> <table class="mceVisualAid" border="0"> <tbody> <tr> <td class="mceVisualAid"><strong>Since <br />2011</strong></td> <td class="mceVisualAid"><strong>PostDoc</strong><br /> Technische Universität München (München, Germany)<br />Laboratory of Catalytic Organic Synthesis<br />Head: Prof. Dr. Lukas Hintermann</td> </tr> <tr> <td class="mceVisualAid" style="width: 70px;"><strong>Since <br />2010  </strong></td> <td class="mceVisualAid"> <p><strong>Teaching Assistant</strong><br />D. I. Mendeleev University of Chemical Technology of Russia (Moscow, Russia)<br />Department of Technology of Organic Substances and Chemical Pharmaceutical Compounds. <br />Subdepartment of Chemistry and Technology of Organic Synthesis.<br />Head: Dr. S. V. Popkov</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2008-<br />2012 </strong></td> <td class="mceVisualAid"> <p><strong>Research Engineer, Junior Research Fellow<br /></strong>N. D. Zelinsky Institute of Organic Chemistry RAS (Moscow, Russia).<br />Laboratory of Fine Organic Synthesis. <br />Head: Prof. S. G. Zlotin</p> </td> </tr> <tr> <td class="mceVisualAid"> <p><strong>2007</strong></p> </td> <td class="mceVisualAid"> <p><strong>Summer Trainee <br /></strong>Institute of Organic Chemistry PAS (Warsaw, Poland). <br />Laboratory of General Organic Chemistry. <br />Head: Prof. M. Mąkosza</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid"><strong>Summer Trainee <br /> </strong>Institute of Organic Chemistry PAS (Warsaw, Poland). <br /> Laboratory of General Organic Chemistry. <br /> Head: Prof. M. Mąkosza</td> </tr> <tr> <td class="mceVisualAid"><strong>2005 - 2008</strong></td> <td class="mceVisualAid"><strong>Research Engineer <br /></strong>A. N. Nesmeyanov Institute of Elementorganic Compounds RAS (Moscow, Russia).<br />Laboratory of Synthesis of Heterocyclic Biological Active Substances. <br />Head: Prof. V. S. Velezheva</td> </tr> <tr> <td class="mceVisualAid"><strong>2004 - 2005</strong></td> <td class="mceVisualAid"><strong>Laboratory Assistant<br /></strong>N. D. Zelinsky Institute of Organic Chemistry RAS (Moscow, Russia). <br />Laboratory of Chemistry of Carbenes and Analogous Intermediates. <br />Head: Acad. M. P. Egorov</td> </tr> </tbody> </table> <h4>Awards ______________________</h4> <table class="mceVisualAid" width="738" border="0"> <tbody> <tr> <td class="mceVisualAid"><strong>2014</strong></td> <td class="mceVisualAid">Listed in the Marquis’ “Who’s Who in the World” Directory of Biographies (31st ed. 2014)</td> </tr> <tr> <td class="mceVisualAid"><strong>2012</strong></td> <td class="mceVisualAid">Best Poster Award. ORCHEM-2012</td> </tr> <tr> <td class="mceVisualAid"><strong>2012</strong></td> <td class="mceVisualAid">Prize of Russian Academy of Sciences for Junior Researchers in the field of General and Technical Chemistry</td> </tr> <tr> <td class="mceVisualAid"><strong>2011</strong></td> <td class="mceVisualAid">Doctor Degree</td> </tr> <tr> <td class="mceVisualAid"><strong>2010</strong></td> <td class="mceVisualAid">Laureate of “The 6th United Congress of Chemical Technology of Youth”</td> </tr> <tr> <td class="mceVisualAid"><strong>2008</strong></td> <td class="mceVisualAid">Master's Diploma: <em>magna cum laude</em></td> </tr> <tr> <td class="mceVisualAid"><strong>2007</strong></td> <td class="mceVisualAid"> <p>Laureate of “Competition of Young Scientists of A. N. Nesmeyanov<br />Institute of Elementorganic Compounds RAS” (up to 35 years)</p> </td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid">Laureate of “Conference of Student Research Works of <br />A.N. Nesmeyanov Institute of Elementorganic Compounds RAS"</td> </tr> <tr> <td class="mceVisualAid"><strong>2006</strong></td> <td class="mceVisualAid">Bachelor's Diploma: <em>magna cum laude </em></td> </tr> <tr> <td class="mceVisualAid" style="width: 70px;"><strong>2002</strong> </td> <td class="mceVisualAid">School leaving certificate: <em>magna cum laude </em></td> </tr> </tbody> </table> <h4 align="left">Selected Publications __________________</h4> <h4><strong>2014 </strong></h4> <p>1. O.V. Maltsev, N.K. Nath, P. Naumov, L. Hintermann. Why is Firefly Oxyluciferin a Notoriously Labile Substance? <em>Angew. Chem. Int. Ed.</em> <strong>2014</strong>, <em><span>53</span></em>, <span>847–850</span>. [<a href="http://dx.doi.org/10.1002/anie.201307972" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <h4><strong>2013 </strong></h4> <p>2. M.W. Jensen,  K. Støchkel, C. Kjær, J.L. Knudsen, Oleg V. Maltsev, L. Hintermann, P. Naumov, B.F. Milne, S.B. Nielsen. Photoinduced dissociation mass spectroscopy of firefly oxyluciferin anions. <em>Int. J. Mass Spectrom.</em> <strong>2013</strong>, DOI: 10.1016/j.ijms.2013.11.012. [<a href="http://dx.doi.org/10.1016/j.ijms.2013.11.012" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>3. O.V. Maltsev, V. Walter, M.J. Brandl, L. Hintermann. Medium Buffer Effects on the Condensation of L-Cysteine and Aryl Nitriles to (<em>R</em>)-2-Aryl-4,5-dihydrothiazole-4-carboxylic Acids. <em>Synthesis </em><strong>2013</strong>, <em>45</em>, 2763. [<a href="http://dx.doi.org/10.1055/s-0033-1339492" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p><a href="http://dx.doi.org/10.1039/C3SC90034G" target="_blank"><img src="../PractChemistry/images/stories/Author/Cover_2.jpg" border="0" width="100" align="right" /></a>4. M. Rebarz, B.-M. Kukovec, O.V. Maltsev, C. Ruckebusch, L. Hintermann, P. Naumov, M. Sliwa. Deciphering the Protonation and Tautomeric Equilibria of Firefly Oxyluciferin by Molecular Engineering and Multivariate Curve Resolution. <em>Chem. Sci.</em> <strong>2013</strong>, <span style="text-decoration: underline;">v.4</span>, 3803. [<a href="http://dx.doi.org/10.1039/C3SC50715G" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>5. K. Støchkel, C.N. Hansen, J. Houmøller, L.M. Nielsen, K. Anggara, M. Linares, P. Norman, F. Nogueira, O.V. Maltsev, L. Hintermann, S.B. Nielsen, P. Naumov, B.F. Milne. On the influence of water on the electronic structure of firefly oxyluciferin anions from absorption spectroscopy of bare and monohydrated ions in vacuo. <em>J. Am. Chem. Soc. </em><strong>2013</strong>, <span style="text-decoration: underline;">v.135</span>, 6485. [<a href="http://dx.doi.org/10.1021/ja311400t" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>6. L. Hintermann, M. Schmitz, O.V. Maltsev, P. Naumov. Organocatalytic Stereoisomerization versus Alkene Isomerization: Catalytic Asymmetric Synthesis of 1-Hydroxy-trans-2,5-diphenylphospholane 1-Oxide. <em>Synthesis </em><strong>2013</strong>, <span style="text-decoration: underline;">v.45</span>, 3, 308. [<a href="http://dx.doi.org/10.1055/s-0032-1316835" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>7. S.G. Zlotin, A.S. Kuherenko, O.V. Maltsev. A.O. Chizhov. Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts. <em>Top. Catal. </em><strong>2013</strong>, <span style="text-decoration: underline;">v.56</span>, 923. [<a href="http://dx.doi.org/10.1007/s11244-013-0056-8" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2012</h4> <p>8. A.S. Kucherenko, D.E. Siyutkin, O.V. Maltsev, S.V. Kochetkov, S.G. Zlotin. Asymmetric organocatalysis: from proline to highly efficient immobilized organocatalysts. <em>Russ. Chem. Bull.</em> <strong>2012</strong>, <span style="text-decoration: underline;">v.61</span>, 7, 1313. [<a href="http://dx.doi.org/10.1007/s11172-012-0177-4" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2011</h4> <p>9.O.V. Maltsev, I.P. Beletskaya, S.G. Zlotin. Organocatalytic Michael and Friedel–Crafts reactions in enantioselective synthesis of biologically active compounds. <em>Russ. Chem. Rev.</em> <strong>2011</strong>, <span style="text-decoration: underline;">v.80</span>, 11, 1067. [<a href="http://dx.doi.org/10.1070/RC2011v080n11ABEH004249" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p><a href="http://dx.doi.org/10.1002/chem.201190109" target="_blank"><img src="../PractChemistry/images/stories/Author/cover_1.gif" border="0" align="right" /></a>10. Maltsev, O.V.; Chizhov, A.O.; Zlotin, S.G. Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts: Deactivation Pathways of Jørgensen–Hayashi-type Catalysts in Asymmetric Michael Reactions. − <em>Chem. Eur. J.</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.17</span>, №22, 6109. [<a href="http://dx.doi.org/10.1002/chem.201100388" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>11. Maltsev, O.V.; Kucherenko, A.S., Zlotin, S.G. O-TMS-α,α-Diphenylprolinol derivatives supported on ionic polymers as recoverable organocatalysts for the asymmetric Michael reactions of carbon acids with α,β-enals. − <em>Mendeleev Commun.</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.21</span>, 146. [<a href="http://dx.doi.org/10.1016/j.mencom.2011.04.011" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2010</h4> <p>12. Maltsev, O.V.; Kucherenko, A.S.; Chimishkyan, A.L.; Zlotin, S.G. a,a-Diarylprolinol-derived Chiral Ionic Liquids − Recoverable Organocatalysts for the Domino Reaction between a,b-Enals and N-Protected Hydroxylamines. − <em>Tetrahedron: Asymmetry</em>, <strong>2010</strong>, <span style="text-decoration: underline;">v.21</span>, 2659 (Highlighted in <em>Synfacts</em>, <strong>2011</strong>, <span style="text-decoration: underline;">v.3</span>, 344 [<a href="http://dx.doi.org/10.1055/s-0030-1259461" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]). [<a href="http://dx.doi.org/10.1016/j.tetasy.2010.10.020" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <p> </p> <p>13. Maltsev, O.V.; Kucherenko, A.S.; Beletskaya, I.P.; Tartakovsky, V.A.; Zlotin, S.G. Chiral Ionic Liquids Bearing O-Silylated a,a-Diphenyl (S)- or (R)-Prolinol Units: Recoverable Organocatalysts for Asymmetric Michael Addition of Nitroalkanes to a,b-Enals. − <em>Eur. J. Org. Chem.</em>, <strong>2010</strong>, 2927. [<a href="http://dx.doi.org/10.1002/ejoc.201000239" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2009</h4> <p>14. Maltsev, O.V.; Kucherenko, A.S.; Zlotin, S.G. O-TMS-a,a-Diphenyl-(S)-prolinol Modified with an Ionic Liquid Moiety: A Recoverable Organocatalyst for the Asymmetric Michael Reaction between a,b-Enals and Dialkyl Malonates. − <em>Eur. J. Org. Chem.</em>, <strong>2009</strong>, 5134. [<a href="http://dx.doi.org/10.1002/ejoc.200900807" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2008</h4> <p>15. Mąkosza, M.; Sulikowski, D.; Maltsev, O.V. Enantioselective Synthesis of (R)-a-(p-Nitroaryl)prolines via Oxidative Nucleophilic Substitution of Hydrogen in Nitroarenes. - <em>Synlett.</em>, <strong>2008</strong>, <span style="text-decoration: underline;">v.11</span>, 1711. [<a href="http://dx.doi.org/10.1055/s-2008-1078483" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>]</p> <h4>2007</h4> <p>16.  Mąkosza, M.; Surowiec, M.; Szczepańska, A.; Sulikowski, D.; Maltsev, O.V. Simple and General Synthesis of a-(p-Nitroaryl) Derivatives of Alanine and Serine. – <em>Synlett.</em>, <strong>2007</strong>, <span style="text-decoration: underline;">v.3</span>, 470. [<a href="http://dx.doi.org/10.1055/s-2007-967952" target="_blank"><span style="text-decoration: underline;"><span style="color: #0066cc;">Link</span></span></a>] </p> </div> </div> </div></div>