Copper-Catalyzed Enantioselective Markovnikov Protoboration of α-Olefins Enabled by a Buttressed N-Heterocyclic Carbene Ligand-Reference-Cited by-同舟云学术

Copper-Catalyzed Enantioselective Markovnikov Protoboration of α-Olefins Enabled by a Buttressed N-Heterocyclic Carbene Ligand

Published:2018-01-08 Issue:5 Volume:57 Page:1376-1380
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Cai Yuan¹²,Yang Xin-Tuo¹,Zhang Shuo-Qing³,Li Feng¹,Li Yu-Qing¹²,Ruan Lin-Xin¹²,Hong Xin³,Shi Shi-Liang¹²^ORCID

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis; Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences; 345 Lingling Road Shanghai 200032 China

2. University of Chinese Academy of Sciences; Beijing 100049 China

3. Department of Chemistry; Zhejiang University; 38 Zheda Road Hangzhou 310027 China

Funder

the Strategic Priority Research Program of the Chinese Academy of Sciences

National Natural Science Foundation of China

1000-Youth Talents Plan

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201711229/fullpdf

Reference93 articles.

1. The development of a simple general procedure for synthesis of pure enantiomers via chiral organoboranes

2. Catalytic Asymmetric Hydroboration: Recent Advances and Applications in Carbon−Carbon Bond‐Forming Reactions

3. The Development of Enantioselective Rhodium-Catalysed Hydroboration of Olefins

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