Enantioselective Rhodium‐Catalyzed Addition of Arylboroxines to N‐Unprotected Ketimines: Efficient Synthesis of Cipargamin-Reference-Cited by-同舟云学术

Enantioselective Rhodium‐Catalyzed Addition of Arylboroxines to N‐Unprotected Ketimines: Efficient Synthesis of Cipargamin

Published:2019-09-24 Issue:45 Volume:58 Page:16119-16123
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Zhu Jinbin¹,Huang Linwei¹,Dong Wei²,Li Naikai²,Yu Xingxin¹,Deng Wei‐Ping¹²,Tang Wenjun¹²^ORCID

Affiliation:

1. Shanghai Key Laboratory of New Drug Design School of Pharmacy East China University of Science and Technology 130 Mei Long Rd Shanghai 200237 China

2. State Key Laboratory of Bio-Organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis Shanghai Institute of Organic Chemistry Chinese Academy of Sciences 345 Ling Ling Rd Shanghai 200032 China

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201910008

Reference92 articles.

1. For recent reviews on α-tertiary amines see:

2. Stereoselective formation of quaternary carbon centers and related functions