Asymmetric catalytic [1,3]- or [3,3]-sigmatropic rearrangement of 3-allyloxy-4<i>H</i>-chromenones and their analogues-Reference-Cited by-同舟云学术

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Asymmetric catalytic [1,3]- or [3,3]-sigmatropic rearrangement of 3-allyloxy-4H-chromenones and their analogues

Published:2024 Issue:28 Volume:15 Page:11005-11012
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Li Yi¹,Ning Lichao¹,Tang Qi¹,Lan Kexin¹,Yang Bingqian¹,Lin Qianchi¹,Feng Xiaoming¹^ORCID,Liu Xiaohua¹^ORCID

Affiliation:

1. Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China

Abstract

A highly efficient asymmetric [1,3]- and [3,3]-O-to-C sigmatropic rearrangement of 3-allyloxy-4H-chromenones and their analogues was developed.

Funder

National Natural Science Foundation of China

Sichuan University

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/SC/D4SC02201G

Reference48 articles.

1. C. M.Rojas , Molecular Rearrangement in Organic Synthesis , Wiley , Hoboken , 2015

2. Recent advances in metal-catalysed asymmetric sigmatropic rearrangements

3. Organoaluminum-promoted Claisen rearrangement of allyl vinyl ethers

4. [1,3]-Sigmatropic rearrangement of allyl vinyl ethers at ambient temperature in 3.0 M lithium, perchlorate-diethyl ether

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