Mechanistic studies on nickel-catalyzed enantioselective [3 + 2] annulation for γ-butenolide synthesis via C–C activation of diarylcyclopropenones-Reference-Cited by-同舟云学术

Mechanistic studies on nickel-catalyzed enantioselective [3 + 2] annulation for γ-butenolide synthesis via C–C activation of diarylcyclopropenones

Published:2021 Issue:12 Volume:8 Page:3023-3031
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Bai Dachang¹²³⁴⁵^ORCID,Liu Song²⁶⁷⁵⁸,Chen Junyan¹²³⁴⁵,Yu Yanjiang¹²³⁴⁵,Wang Manman¹²³⁴⁵,Chang Junbiao¹²³⁴⁵,Lan Yu²⁶⁷⁵^ORCID,Li Xingwei¹²³⁴⁵^ORCID

Affiliation:

1. Henan Key Laboratory of Organic Functional Molecule and Drug Innovation

2. School of Chemistry and Chemical Engineering

3. Henan Normal University

4. Xinxiang 453007

5. China

6. Chongqing University

7. Chongqing 400030

8. Chongqing Key Laboratory of Environmental Materials and Remediation Technologies

Abstract

Detailed mechanistic studies on Ni-catalyzed C–C activation of cyclopropenones, and enantioselective [3 + 2] annulation with α-CF₃ enones or 1,2-diones toward the efficient synthesis of γ-butenolides.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Henan Province

China Postdoctoral Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00322D

Reference69 articles.

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3. Recent Methodologies That Exploit C–C Single-Bond Cleavage of Strained Ring Systems by Transition Metal Complexes

4. “Cut and Sew” Transformations via Transition-Metal-Catalyzed Carbon–Carbon Bond Activation

5. Metal–Organic Cooperative Catalysis in C–H and C–C Bond Activation

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