Silver-catalyzed regioselective 1,6-hydroarylation of <i>para</i>-quinone methides with anilines and phenols-Reference-Cited by-同舟云学术

Silver-catalyzed regioselective 1,6-hydroarylation of para-quinone methides with anilines and phenols

Published:2022 Issue:14 Volume:9 Page:3807-3817
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Xiong Biquan¹²^ORCID,Xu Shipan¹,Xu Weifeng¹,Liu Yu¹^ORCID,Zhang Limin²,Tang Ke-Wen¹^ORCID,Yin Shuang-Feng³^ORCID,Wong Wai-Yeung²^ORCID

Affiliation:

1. Department of Chemistry and Chemical Engineering, Hunan Institute of Science and Technology, Yueyang, 414006, P. R. China

2. Department of Applied Biology and Chemical Technology and Research Institute for Smart Energy, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, P. R. China

3. Advanced Catalytic Engineering Research Center of the Ministry of Education, State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, Hunan Province, P. R. China

Abstract

A novel and facile method for the Ag-catalyzed regioselective 1,6-hydroarylation of para-quinone methides (p-QMs) with anilines and phenols has been established, and a broad range of anilines (primary secondary, tertiary), phenols and p-QMs are well tolerated.

Funder

Natural Science Foundation of Hunan Province

Scientific Research Foundation of Hunan Provincial Education Department

CAS-Croucher Funding Scheme for Joint Laboratories

Hong Kong Polytechnic University

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00541G