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プロフィール詳細
Dr. Yury M.に依頼
United States
Medicinal Chemistry/Drug Development/Organic Synthesis expert with 10+ years of experience in chemical R&D
プロフィール概要
専門分野
サービス
Writing
Technical Writing
Research
Scientific and Technical Research,
Systematic Literature Review
Consulting
Scientific and Technical Consulting,
Manufacturing Consulting
Data & AI
Data Cleaning
Product Development
Stability/Shelf Life Testing,
Product Evaluation,
Material Sourcing,
Product Validation,
Manufacturing,
Concept Development
職務経験
Postdoctoral Research Associate
Los Alamos National Laboratory
10月 2017 - 現在 ![]()
Senior Research and Development Chemist
OPKO Health / Finetech Pharmaceutical
8月 2022 - 10月 2025
Postdoctoral Research Associate
Los Alamos National Laboratory
10月 2017 - 6月 2022 ![]()
Postdoctoral Fellow
University of Utah
12月 2014 - 12月 2016 ![]()
学歴
Ph.D. (Schulich Faculty of Chemistry)
Technion Israel Institute of Technology
10月 2007 - 8月 2014 ![]()
M.Sc. (Chemistry)
N. I. Lobachevsky State University of Nizhny Novgorod
9月 2004 - 7月 2007 ![]()
B.Sc. (Chemistry)
N. I. Lobachevsky State University of Nizhny Novgorod
9月 2001 - 6月 2004 ![]()
認定資格
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DL-170 Specialized Course on the Essentials of Patents
WIPO - World Intellectual Property Organization
https://welc.wipo.int/lms/verify/index.php?q=sM3ZpqCIL49月 2025 - 現在
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Artificial Intelligence in Pharma and Biotech
Massachusetts Institute of Technology, Sloan School of Management
https://api.accredible.com/v1/frontend/credential_website_embed_image/certificate/1308898351月 2025 - 現在
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Drug Development Product Management
UC San Diego on Coursera
https://coursera.org/share/a33832e056c14787cb04b9bcc97e553b8月 2024 - 現在
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Drug Hunting: The Science of Making New Medicines
Novartis (on Coursera)
https://www.coursera.org/account/accomplishments/specialization/48P99QLQHTPS7月 2024 - 現在
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Drug and Medical Device Development: A Strategic Approach
Massachusetts Institute of Technology, MIT xPRO program
https://certificates.emeritus.org/56e20641-e651-4dd2-bd13-3af2332cfed7#acc.xCRKshSk1月 2023 - 現在
出版物
JOURNAL ARTICLE
Yury Minko, Taylor V. Fetrow, Shikha Sharma, Brenna K. Cashman, Aaron M. Tondreau (2024). Flexible interactions of the rare-earth elements Y, La, and Lu with phosphorus in metallacyclohexane rings . Chemical Science.
Pavel A. Dub and Rami J. Batrice and John C. Gordon and Brian L. Scott and Yury Minko and Jurgen G. Schmidt and Robert F. Williams(2020). Engineering Catalysts for Selective Ester Hydrogenation . Organic Process Research & Development. 24. (3). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 415--442. American Chemical Society ({ACS})
Yury Minko, Jing-Yao Guo, Celine B. Santiago, Matthew S. Sigman(2017). Developing Comprehensive Computational Parameter Sets To Describe the Performance of Pyridine-Oxazoline and Related Ligands . ACS Catalysis. 7. (6). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 4144--4151. American Chemical Society ({ACS})
Guo, J.-Y., Minko, Y., Santiago, C.B., Sigman, M.S.(2017). Developing Comprehensive Computational Parameter Sets to Describe the Performance of Pyridine-Oxazoline and Related Ligands . ACS Catalysis. 7. (6). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 4144-4151.
Yury Minko, Zackaria Nairoukh, Gunda G. K. S. Narayana Kumar, Ilan Marek(2017). Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres . Chemical Science. 8. (1). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 627--630. Royal Society of Chemistry ({RSC})
Nairoukh, Z., Kumar, G.G.K.S.N., Minko, Y., Marek, I.(2016). Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres . Chemical Science. 8. (1). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 627-630.
Yury Minko, Ilan Marek, Morgane Pasco, Tom Mejuch, Noga Gilboa, Helena Chechik, Jaya P. Das(2014). All-Carbon Quaternary Stereogenic Centers in Acyclic Systems through the Creation of Several C–C Bonds per Chemical Step . Journal of the American Chemical Society. 136. (7). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 2682--2694. American Chemical Society ({ACS})
Marek, I., Minko, Y., Pasco, M., Mejuch, T., Gilboa, N., Chechik, H., Das, J.P.(2014). All-carbon quaternary stereogenic centers in acyclic systems through the creation of several C-C bonds per chemical step . Journal of the American Chemical Society. 136. (7). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 2682-2694.
Yury Minko, Ilan Marek(2014). Oxenoids in organic synthesis . Org. Biomol. Chem. 12. (10). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 1535--1546. Royal Society of Chemistry ({RSC})
Minko, Y., Marek, I.(2014). Oxenoids in organic synthesis . Organic and Biomolecular Chemistry. 12. (10). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 1535-1546.
Yury Minko, Ilan Marek(2014). Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentres . Chem. Commun. 50. (84). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 12597--12611. Royal Society of Chemistry ({RSC})
Minko, Y., Marek, I.(2014). Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentres . Chemical Communications. 50. (84). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 12597-12611.
Yury Minko, Morgane Pasco, Helena Chechik, Ilan Marek(2013). Regio- and stereoselective carbometallation reactions ofN-alkynylamides and sulfonamides . Beilstein Journal of Organic Chemistry. 9. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 526--532. Beilstein Institut
Yury Minko, Morgane Pasco, Lukas Lercher, Ilan Marek(2013). Stereodefined trisubstituted enolates as a unique entry to all-carbon quaternary stereogenic centers in acyclic systems . Nature Protocols. 8. (4). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 749--754. Springer Nature
Minko, Y., Pasco, M., Lercher, L., Marek, I.(2013). Stereodefined trisubstituted enolates as a unique entry to all-carbon quaternary stereogenic centers in acyclic systems . Nature Protocols. 8. (4). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 749-754.
Minko, Y., Pasco, M., Chechik, H., Marek, I.(2013). Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides . Beilstein Journal of Organic Chemistry. 9. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 526-532.
Yury Minko, Morgane Pasco, Lukas Lercher, Mark Botoshansky, Ilan Marek(2012). Forming all-carbon quaternary stereogenic centres in acyclic systems from alkynes . Nature. 490. (7421). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 522--526. Springer Nature
Minko, Y., Pasco, M., Lercher, L., Botoshansky, M., Marek, I.(2012). Forming all-carbon quaternary stereogenic centres in acyclic systems from alkynes . Nature. 490. (7421). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 522-526.
PREPRINT
Yury Minko, Shounak Banerjee, Elizabeth S Anaya, Zachary J Sasiene, Jurgen G Schmidt, Charlie E M Strauss, Geoffrey S Waldo (2022). Configurational entropy-based screening and selection of hydrophilic polymers using the tripartite split green fluorescent protein .
OTHER
Yury Minko, Ilan Marek(2014). Advances in Carbolithiation . Lithium Compounds in Organic Synthesis. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 329--350. Wiley-{VCH} Verlag {GmbH} {\&} Co. {KGaA}
Yury Minko, Ilan Marek(2013). Carbometallation Reactions . Metal-Catalyzed Cross-Coupling Reactions and More. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 763--874. Wiley-{VCH} Verlag {GmbH} {\&} Co. {KGaA}
BOOK CHAPTER
Minko, Y., Marek, I.(2014). Advances in Carbolithiation . Lithium Compounds in Organic Synthesis: From Fundamentals to Applications. 9783527333431. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 329-350.
Marek, I., Minko, Y.(2013). Carbometallation Reactions . Metal Catalyzed Cross-Coupling Reactions and More. 3. Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 763-874.