† State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, P. R. China
‡ Laboratory of Molecular Recognition and Synthesis, Department of Chemistry, Zhejiang University, Hangzhou 310027, Zhejiang, P. R. China
Acc. Chem. Res., 2014, 47 (4), pp 989–1000
DOI: 10.1021/ar4002069
Publication Date (Web): January 30, 2014
Electrophilic Addition and Cyclization Reactions of Allenes
Laboratory of Molecular Recognition and Synthesis, Department of Chemistry, Zhejiang University, Hangzhou 310027, Zhejiang, P.R. China, and State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, P.R. China
Acc. Chem. Res., 2009, 42 (10), pp 1679–1688
DOI: 10.1021/ar900153r
Publication Date (Web): July 15, 2009
Transition Metal-Catalyzed/Mediated Reaction of Allenes with a Nucleophilic Functionality Connected to the α-Carbon Atom
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, People's Republic of China
Acc. Chem. Res., 2003, 36 (9), pp 701–712
DOI: 10.1021/ar020133k
Publication Date (Web): June 20, 2003
施敏:三篇
Gold-Catalyzed Tandem Reactions of Methylenecyclopropanes and Vinylidenecyclopropanes
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, People’s Republic of China
Acc. Chem. Res., 2014, 47 (3), pp 913–924
DOI: 10.1021/ar400159r
Publication Date (Web): October 30, 2013
Rapid Generation of Molecular Complexity in the Lewis or Brønsted Acid-Mediated Reactions of Methylenecyclopropanes
† State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P. R. China
‡ College of Chemistry and Materials Engineering, Wenzhou University, Chashan University Town, Wenzhou, Zhejiang Province 325035, P. R. China.
Acc. Chem. Res., 2012, 45 (4), pp 641–652
DOI: 10.1021/ar200237z
Publication Date (Web): December 13, 2011
Multifunctional Chiral Phosphine Organocatalysts in Catalytic Asymmetric Morita−Baylis−Hillman and Related Reactions
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032 China
Acc. Chem. Res., 2010, 43 (7), pp 1005–1018
DOI: 10.1021/ar900271g
Publication Date (Web): March 16, 2010
马大为:两篇
Intramolecular Dearomative Oxidative Coupling of Indoles: A Unified Strategy for the Total Synthesis of Indoline Alkaloids
State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China
Acc. Chem. Res., 2015, 48 (3), pp 702–711
DOI: 10.1021/ar5004303
Publication Date (Web): February 10, 2015
Copper/Amino Acid Catalyzed Cross-Couplings of Aryl and Vinyl Halides with Nucleophiles†
State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China
Acc. Chem. Res., 2008, 41 (11), pp 1450–1460
DOI: 10.1021/ar8000298
Publication Date (Web): August 13, 2008
北京大学
席振峰:两篇
Zirconocene and Si-Tethered Diynes: A Happy Match Directed toward Organometallic Chemistry and Organic Synthesis
Beijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China
Acc. Chem. Res., 2011, 44 (7), pp 541–551
DOI: 10.1021/ar200078e
Publication Date (Web): May 25, 2011
1,4-Dilithio-1,3-dienes: Reaction and Synthetic Applications
Beijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China
Acc. Chem. Res., 2010, 43 (10), pp 1342–1351
DOI: 10.1021/ar1000583
Publication Date (Web): July 15, 2010
南开大学
周其林:两篇
Transition-Metal-Catalyzed Enantioselective Heteroatom–Hydrogen Bond Insertion Reactions
† Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry,University of Science and Technology of China, Hefei 230026, China
‡Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300072, China
Acc. Chem. Res., 2014, 47 (8), pp 2365–2377
DOI: 10.1021/ar500101a
Publication Date (Web): June 9, 2014
Brønsted-Acid-Catalyzed Asymmetric Multicomponent Reactions for the Facile Synthesis of Highly Enantioenriched Structurally Diverse Nitrogenous Heterocycles
Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, University of Science and Technology of China, Hefei 230026, P. R. China
School of Chemistry and Chemical Engineering, Xuzhou Normal University, Xuzhou 221116, P. R. China