Hydroquinine-catalyzed asymmetric 1,4-hydrophosphination of in situ generated aza-o-quinone methides with H-phosphine oxides-Reference-Cited by-同舟云学术

Hydroquinine-catalyzed asymmetric 1,4-hydrophosphination of in situ generated aza-o-quinone methides with H-phosphine oxides

Published:2021 Issue:18 Volume:8 Page:5064-5070
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Yang Fuxing¹^ORCID,Zhou Xingcui¹,Wei Yongquan¹,Wang Lisheng¹²,Jiang Jun¹³^ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering, Guangxi University, Nanning, 530004, P. R. China

2. Medical College, Guangxi University, Nanning, 530004, P. R. China

3. Guangxi Key Laboratory of Electrochemical Energy Materials, Nanning, Guangxi 530004, P. R. China

Abstract

An organocatalytic enantioselective 1,4-addition of H-phosphine oxides to in situ generated aza-o-quinone methides has been successfully established using hydroquinine.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangxi Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00823D

Reference69 articles.

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4. Recent advances in the application of Diels–Alder reactions involving o-quinodimethanes, aza-o-quinone methides and o-quinone methides in natural product total synthesis

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