Highly regioselective C–H carbonylation of alkenes with phenyl formate<i>via</i>aryl to vinyl 1,4-palladium migration-Reference-Cited by-同舟云学术

Highly regioselective C–H carbonylation of alkenes with phenyl formateviaaryl to vinyl 1,4-palladium migration

Published:2023 Issue:6 Volume:10 Page:1537-1543
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Ye Tao¹²,Cheng Fangyuan¹,Zhang Jian¹,Liu Yang-Zi¹^ORCID,Wang Quannan¹,Deng Wei-Ping¹²^ORCID

Affiliation:

1. Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Department of Chemistry, Zhejiang Normal University, 688 Yingbin Road, Jinhua 321004, P. R. China

2. Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China

Abstract

A novel approach to synthesize β,β-diaryl substituted α,β-unsaturated esters in high efficiency and with excellent regio- and stereoselectivities was developed.

Funder

National Key Research and Development Program of China

Zhejiang Normal University

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00066D

Reference75 articles.

1. Chalcone: A Privileged Structure in Medicinal Chemistry