Enantioselective Hydroesterificative Cyclization of 1,6-Enynes to Chiral γ-Lactams Bearing a Quaternary Carbon Stereocenter-Reference-Cited by-同舟云学术

Enantioselective Hydroesterificative Cyclization of 1,6-Enynes to Chiral γ-Lactams Bearing a Quaternary Carbon Stereocenter

Published:2021-04-28 Issue:9 Volume:23 Page:3561-3566
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Ren Xinyi¹,Tang Lin¹,Shen Chaoren¹^ORCID,Li Huimin¹,Wang Peng¹^ORCID,Dong Kaiwu¹^ORCID

Affiliation:

1. Chang-Kung Chuang Institute, and Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, P.R. China

Funder

East China Normal University

National Natural Science Foundation 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.1c00952

Reference57 articles.

1. Recent progress towards transition metal-catalyzed synthesis of γ-lactams

2. Biologically active γ-lactams: synthesis and natural sources

3. Advances toward the Synthesis of Functionalized γ-Lactams

4. Highly Enantioselective Reductive Cyclization of Acetylenic Aldehydes via Rhodium Catalyzed Asymmetric Hydrogenation

5. Asymmetric Synthesis of β-Substituted γ-Lactams via Rhodium/Diene-Catalyzed 1,4-Additions: Application to the Synthesis of (R)-Baclofen and (R)-Rolipram

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