Construction of Vicinal All-Carbon Stereogenic Centers via Copper-Catalyzed Asymmetric Decarboxylative Propargylation: Enantio- and Diastereoselective Synthesis of Substituted Spirolactones-Reference-Cited by-同舟云学术

Construction of Vicinal All-Carbon Stereogenic Centers via Copper-Catalyzed Asymmetric Decarboxylative Propargylation: Enantio- and Diastereoselective Synthesis of Substituted Spirolactones

Published:2023-01-11 Issue:2 Volume:25 Page:410-415
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zuo Sheng¹²,Tao Yuan¹²,Liu Zhigang¹²,Zhang Ke¹²,Zhang Luyun¹²,Ning Yingtang¹²,Chen Fen-Er¹²^ORCID

Affiliation:

1. Engineering Center of Catalysis and Synthesis for Chiral Molecules, Fudan University, 200433 Shanghai, China

2. Shanghai Engineering Center of Industrial Catalysis for Chiral Drugs, 200433 Shanghai, China

Funder

Ministry of Science and Technology of the People's Republic of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c04113

Reference34 articles.

1. Enantioselective formation of quaternary carbon stereocenters in natural product synthesis: a recent update

2. Catalytic enantioselective construction of vicinal quaternary carbon stereocenters

3. Contiguous stereogenic quaternary carbons: A daunting challenge in natural products synthesis

4. Organo-Cation Catalyzed Asymmetric Homo/Heterodialkylation of Bisoxindoles: Construction of Vicinal All-Carbon Quaternary Stereocenters and Total Synthesis of (−)-Chimonanthidine

5. Construction of Multiple, Contiguous Quaternary Stereocenters in Acyclic Molecules by Lithiation-Borylation

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