Efficient Synthesis of (−)-Corynoline by Enantioselective Palladium-Catalyzed α-Arylation with Sterically Hindered Substrates-Reference-Cited by-同舟云学术

Efficient Synthesis of (−)-Corynoline by Enantioselective Palladium-Catalyzed α-Arylation with Sterically Hindered Substrates

Published:2018-08-28 Issue:38 Volume:130 Page:12508-12512
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Rao Xiaofeng¹,Li Naikai¹,Bai Heng¹,Dai Chaodi¹,Wang Zheng²,Tang Wenjun¹^ORCID

Affiliation:

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

2. Informatics and Technology; Astra Zeneca China; Shanghai China

Funder

the Chinese Academy of Sciences

Chinese Academy of Sciences

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

K.C. Wong Education Foundation

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201807302/fullpdf

Reference92 articles.

1. Catalytic enantioselective synthesis of quaternary carbon stereocentres

2. Direct construction of vicinal all-carbon quaternary stereocenters in natural product synthesis

3. All-carbon quaternary centers in natural products and medicinal chemistry: recent advances

4. Direct construction of vicinal all-carbon quaternary stereocenters in natural product synthesis

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