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个人简介

1995年毕业于华东理工大学精细化工系;1998年于中国科学院上海有机化学研究所获硕士学位;2003年于美国宾夕法尼亚州立大学获博士学位;2003-2005 年在美国Scripps 研究所从事博士后研究;2005-2009年在美国Boehringer Ingelheim药业公司药物工艺部门(Chemical Development) 任高级科学家(Senior Scientist), 在2009-2011年间任首席科学家 (Principal Scientist);2011年7月起任中科院上海有机化学研究所研究员、课题组长;同时兼任上海科技大学物质学院教授、博导、杭州高等研究院首席教授及华东理工大学药学院博导,2015年获中国均相催化青年奖,2017年获国家杰出青年基金资助。2018年入选科技部中青年科技创新领军人才。2019年获药明康德生命化学研究奖学者奖。

研究领域

1.发展高效、实用、绿色的催化反应方法学 过渡金属催化是当代有机合成化学中最活跃的领域之一。在过渡金属参与的催化反应中,过渡金属催化剂是整个反应过程的关键,而配体的特性包括电子效应,立体效应,和空间效应直接影响了催化剂的活性和选择性。手性膦配体的发展极大地推动了整个不对称催化领域。在过去的几年中,我们研究小组设计和发展了一系列有显著结构特征的P-手性膦配体在大位阻偶联、不对称偶联、不对称环化、以及不对称氢化中表现出优异的效率,为复杂天然产物和药物的高效合成提供了实用、绿色的催化反应方法学 2. 复杂天然产物全合成 利用我们研究小组发展的合成方法学,开展对一些有重要生理活性天然产物的高效全合成或骨架合成,并进行相关药化研究。以下是我们研究小组已完成的一些天然产物 3. 药物绿色合成 发展能工业化的、高效、经济的新反应或合成策略,实施对药物分子或农药的新工艺研究,非常愿意与有诚意的企业共同研发药物的绿色合成工艺

近期论文

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Lv, Y.; Liao, H.; Tang, W.* “Synthesis of a Sitagliptin Intermediate via Ruthenium-Catalyzed Asymmetric Hydrogenation of Enamine Ester”.Chin. J. Org. Chem. 2024, . Lin, Y.; Xu, G.;* Tang, W.* “Chiral Polymeric Diamine Ligands for Iridium-Catalyzed Asymmetric Transfer Hydrogenation”.J. Am Chem. Soc. 2024, . Cao, Z.; He, D.; Tang, W.* “Catalysis and Synthesis Enabled by P-Chiral Dihydrobenzooxaphosphole Ligands”.Org. Process Res. Dev. 2024, . Bai, H. (1st co-author); Gu, W.(1st co-author); Zhao, D.; Xu, G.;* Tang, W.* “Synthesis of dydrogesterone by aromatization-dearomatization strategy”.Green Synthesis and Catalysis. 2023, . Peng, H.(1st co-author); Zhao, D.(1st co-author); Tang, W.;* Peng, A.* “Dienediamine: A Safe Herbicide as Paraquat Surrogate”.Mol. Plant. 2023, 16, 1962-1975. Liu, Z.; Gao, B.; Chernichenko, K.; Yang, H.;* Lemaire, S.;* Tang, W.* “Enantioselective C-H Arylation for Axially Chiral Heterobiaryls”.Org. Lett. 2023, 25, 7004-7008. Yang, H.(1st co-author); Yu, H.(1st co-author); Stolarzewicz. I. A.;* Tang, W.* “Enantioselective transformations in the synthesis of therapeutic agents”.Chem. Rev. 2023, . Sun, J.; Chen, Y.; Ragab. S. S.; Gu, W.; Tang, Z.; Tang, Y.; Tang, W.* “Total Syntheses of Polyhydroxylated Steroids by an Unsaturation-Functionalization Strategy”Angew. Chem., Int. Ed. 2023, 62, e202303639. Zhou, M.(1st co-author); Lin, Y.(1st co-author); Chen, X.-X.(1st co-author); Xu, G.;* Chung, L. W.;* Tang, W.* "Asymmetric Synthesis of Vicinal Tetrasubstituted Diamines via Reductive Coupling of Ketimines Templated by Chiral Diborons".Angew. Chem., Int. Ed. 2023, 62, e202300334. Zhu, Y.; Dong, W.; Tang, W.* "Palladium-Catalyzed Cross-Couplings in the Synthesis of Agrochemicals".Advanced Agrochem 2022, 1, 125-138. Li, B.; Luo, B.; Yang, H.;* Tang, W.* "Heck Reaction of N-Heteroaryl Halides for Concise Synthesis of Chiral α-Heteroaryl-substituted Heterocycles".Angew. Chem., Int. Ed. 2022, 61, e202209087. Yang, H.; Tang, W.* “Enantioselective Construction of ortho-Sulfur- or Nitrogen-Substituted Axially Chiral Biaryls and Asymmetric Synthesis of Isoplagiochin D”.Nat. Commun. 2022, 13, 4577. Kang, X.; Qian, C.; Yang, H.; Shi, J.;* Claverie, J.;* Tang, W.* “Protecting-group-free enantioselective tandem allylic substitution of o-phenylenediamines and o-aminophenols”.Green Synthesis and Catalysis. 2022, 3, 185-189. Li, Z.; Xu, R.; Guo, H.; Yang, H.; Xu, G.; Shi, E.* Xiao, J.* Tang, W.* “Enantioselective Rhodium-Catalyzed Hydrogenation of (Z)‑N‑Sulfonyl-α-Dehydroamido Boronic Esters”.Org. Lett. 2022, 24, 714-719. Li, B.; Luo, B.; Blakemore, C. A.;* Smith, A. C.; Widlicka, D. W.; Berritt, S.; Tang, W.* “Synthesis of α-Heteroaryl Propionic Esters by Palladium-Catalyzed α-Heteroarylation of Silyl Ketene Acetals”.Org. Lett. 2021, 23, 6439-6443. Tian, W.; Li, B.; Tian, D.; Tang, W.* “Regioselective 2-alkylation of indoles with α-bromo esters catalyzed by Pd/P,P=O system”.Chin. Chem. Lett. 2022, 33, 197-200. Sun, J.; Gu, W.; Yang, H.;* Tang, W.* “Enantioselective total synthesis of parnafungin A1 and 10a-epi-hirtusneanine”.Chem. Sci. 2021, 12, 10313-10320. Wan, F.; Wang, N.; Zhu, Y.; Tang, C.; Claverie, J. P.;* Tang, W.* “Enantioselective Hydrogenation of Cyclic Tetrasubstituted-Olefinic Dehydroamino Acid Derivatives”.Chem. Commun. 2021, 57, 5546-5549. Peng, H.; Li, T.; Tian, D.; Yang, H.; Xu, G.; Tang, W.* “Metal-Free Reduction of Unsaturated Carbonyls, Quinones, and Pyridinium Salts with Tetrahydroxydiboron/Water”.Org. Biomol. Chem. 2021, 19, 4327-4337. Xu, R.; Gao, Z.,; Yu, Y.; Tang, Y.; Tian, D.; Chen, T.; Chen, Y. ; Xu G. Shi, E.; Tang, W.* "A Facile and Practical Preparation of P-Chiral Phosphine Oxides".Chem. Commun. 2021, 57, 3335-3338. Wu, T.; Zhou, Q.; Tang, W.* “Enantioselective α‐Carbonylative Arylation for Facile Construction of Chiral Spirocyclic β,β'‐Diketones".Angew. Chem., Int. Ed. 2021, 60, 9978-9983. Sun, J.; Yang, H.;* Tang, W.* "Recent advances in total syntheses of complex dimeric natural products".Chem. Soc. Rev. 2021, 50, 2320-2336. Tian, D,; Xu, R,; Zhu, J.; Huang, J.; Dong, W.; Claverie, J.; Tang, W.* "Asymmetric Hydroesterification of Diarylmethyl Carbinols".Angew. Chem., Int. Ed. 2021, 60, 6305-6309. Tang, W.* "Author Profile".Angew. Chem., Int. Ed. 2020, 59, 7988. Wan, F.; Tang, W.* "Phosphorus Ligands from the Zhang Lab: Design, Asymmetric Hydrogenation, and Industrial Applications".Chin. J. Chem. 2021, 39, 954-968. Aliyu, M.; Li, B.; Yang, H.; Tang, W.* "Palladium-catalyzed reductive cross-coupling between α-bromo carboxamides and terminal alkynes".Org. Chem. Front. 2020, 7, 3505-3508. i, K.; Nie, M.; Tang, W.* "Synthesis of α-tertiary allylsilanes by palladium-catalyzed hydrosilylation of 1,1-disubstituted allenes".Green Synthesis and Catalysis. 2020, 1, 171-174. u, H.; Yang, H.;* Shi, E.;* Tang, W.* “Development and Clinical Application of Phosphorus-Containing Drugs".Med. Drug Discov. 2020, 8, 100063. u, T.; Tang, W.* “Construction of Bridged Polycyclic Skeletons via Transition‐Metal Catalyzed Carbon‐Carbon Bond‐Forming Reaction".Chem. Eur. J. 2021, 27, 3944-3956. i, B.; Aliyu, M.; Gao, Z.; Li, T.; Dong, W.; Shi, E.* Tang, W.* “General Synthesis of Chiral α,α-Diaryl Carboxamides by Enantioselective Palladium-Catalyzed Cross-Coupling".Org. Lett. 2020, 13, 4974-4978. u, T.; Kang, X.; Bai, H.; Xiong, W.; Xu, G.; Tang, W.* “Enantioselective Construction of Spiro Quaternary Carbon Stereocenters via Pd-Catalyzed Intramolecular α-Arylation".Org. Lett. 2020, 22, 4602-4607. Qian, C.; Tang, W.* "A Versatile Synthesis of Vinyl-Substituted Heterocycles via Regio- and Enantioselective Pd-Catalyzed Tandem Allylic Substitution".Org. Lett. 2020, 22, 4483-4488. Zhou, M.; Li, K.; Chen, D.; Xu, R.; Xu, G.* Tang, W.* "Enantioselective Reductive Coupling of Imines Templated by Chiral Diboron".J. Am. Chem. Soc. 2020, 142, 10337-10342. Xu, R.H.; Yang, H.; Tang, W.*“Efficient Synthesis of Chiral Drugs Facilitated by P-Chiral Phosphorus Ligands”.Chin. J. Org. Chem. 2020, 14, 581. Liu, Z.; Li, T.; Zhao, J.; Tang, W.* “A substituted tricyclohexylphosphane with ‘conformational lock’”.Tetrahedron. 2020, 76, 131216. Yang, H.; Sun, J.; Gu, W.; Tang, W.* "Enantioselective Cross-Coupling for Axially Chiral Tetra-ortho-Substituted Biaryls and Asymmetric Synthesis of Gossypol".J. Am. Chem. Soc. 2020, 142, 8036–8043. Mu, X.; Yu, H.; Peng, H.; Xiong, W.; Wu, T.; Tang, W.* "Expedite Construction of Various Bridged Polycyclic Skeletons by Palladium-Catalyzed Dearomatization".Angew. Chem., Int. Ed. 2020, 59, 8143-8147. Wu, T; Xu, G; Tang, W.* “P-Chiral Phosphorus Ligands for Cross-Coupling and Asymmetric Hydrogenation Reactions”.Aldrichimica Acta 2020, 53, 27-35. Li, C.; Ragab. S.S.; Liu, G.;* Tang, W.* "Enantioselective Formation of Quaternary Carbon Stereocenters in Natural Product Synthesis: A Recent Update".Nat. Prod. Rep. 2020, 37, 276. Zhu, J.; Huang, L.; Dong, W.; Li, N.; Yu, X.; Deng, W.*; Tang,W.* "Enantioselective Rhodium-Catalyzed Addition of Arylboroxines to N-Unprotected Ketimines: Efficient Synthesis of Cipargamin".Angew. Chem., Int. Ed. 2019, 58, 16119-16123. Li, C.(1st co-author); Wan, F.(1st co-author); Chen, Y.; Peng, H.; Tang, W.*; Yu, S.*; McWilliams, J. C.*, Mustakis, J.; Samp, L.; Maguire, R. J. "Stereoelectronic Effects in Ligand Design: Enantioselective RhodiumCatalyzed Hydrogenation of Aliphatic Cyclic Tetrasubstituted Enamides and Concise Synthesis of (R)-Tofacitinib".Angew. Chem., Int. Ed. 2019, 58, 13573-13583.

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