Dinuclear zinc-catalyzed enantioselective formal [3 + 2] cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with low reactivity aurone derivatives-Reference-Cited by-同舟云学术

Dinuclear zinc-catalyzed enantioselective formal [3 + 2] cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with low reactivity aurone derivatives

Published:2021 Issue:39 Volume:19 Page:8492-8496
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Rui-Li¹,Jia Shi-Kun¹,Guo Ya-Jun¹,Yi Yang¹,Hua Yuan-Zhao¹,Lu Hui-Jie¹,Wang Min-Can¹^ORCID

Affiliation:

1. Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou 450001, China

Abstract

Highly enantioselective formal [3 + 2] cycloaddition via a Brønsted base and Lewis acid cooperative activation model.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01599K

Reference54 articles.

1. Highly Enantioselective Ag(I)-Catalyzed [3 + 2] Cycloaddition of Azomethine Ylides

2. Enantioselective Copper-Catalyzed 1,3-Dipolar Cycloadditions

3. Enantioselective Silver-Catalyzed Transformations

4. Catalytic asymmetric construction of spiropyrrolidines via 1,3-dipolar cycloaddition of azomethine ylides

5. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides

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