Copper(i)-catalyzed highly enantioselective [3 + 3]-cycloaddition of γ-alkyl enoldiazoacetates with nitrones-Reference-Cited by-同舟云学术

Copper(i)-catalyzed highly enantioselective [3 + 3]-cycloaddition of γ-alkyl enoldiazoacetates with nitrones

Published:2020 Issue:13 Volume:7 Page:1653-1657
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Dong Kuiyong¹²³⁴⁵,Xu Xinfang⁵⁶⁷⁸⁹^ORCID,Doyle Michael P.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. University of Texas at San Antonio

3. San Antonio

4. USA

5. Key Laboratory of Organic Synthesis of Jiangsu Province

6. College of Chemistry

7. Chemical Engineering and Materials Science

8. Soochow University

9. Suzhou 215123

Abstract

Chiral copper(i) catalysts are preferred over chiral dirhodium(ii) catalysts for [3 + 3]-cycloaddition reactions of γ-alkyl-substituted enoldiazoacetates compounds with nitrones.

Funder

National Science Foundation

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QO/D0QO00539H

Reference28 articles.

1. 1,3-Dipolar Cycloadditions. Past and Future

2. Asymmetric 1,3-Dipolar Cycloaddition Reactions

3. Asymmetric 1,3-dipolar cycloadditions

4. Green Protocols in Heterocycle Syntheses via 1,3-Dipolar Cycloadditions

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