Stereoselective Cyclopropanation of Multisubstituted Enesulfinamides: Asymmetric Construction of α-Tertiary Cyclopropylamine Derivatives Containing β-Quaternary Stereocenters-Reference-Cited by-同舟云学术

Stereoselective Cyclopropanation of Multisubstituted Enesulfinamides: Asymmetric Construction of α-Tertiary Cyclopropylamine Derivatives Containing β-Quaternary Stereocenters

Published:2024-03-21 Issue:13 Volume:26 Page:2606-2611
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhu Chong-Lin¹²,Lu Chong-Dao¹³²^ORCID

Affiliation:

1. School of Chemical Science and Technology, Yunnan University, Kunming, Yunnan 650091, China

2. Southwest United Graduate School, Kunming, Yunnan 650092, China

3. School of Health, Jiangxi Normal University, Nanchang, Jiangxi 330022, China

Funder

Double Thousand Plan of Jiangxi Province

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00614

Reference49 articles.

1. An Overview of Phenylcyclopropylamine Derivatives: Biochemical and Biological Significance and Recent Developments

2. The “Cyclopropyl Fragment” is a Versatile Player that Frequently Appears in Preclinical/Clinical Drug Molecules

3. Selective Carbon–Carbon Bond Cleavage of Cyclopropylamine Derivatives

4. Cyclopropanation Strategies in Recent Total Syntheses

5. Selective Carbon-Carbon Bond Cleavage for the Stereoselective Synthesis of Acyclic Systems

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