Recent Advances in the Asymmetric Doyle–Kirmse Reaction

Author:

Teng Ming-Yu1,Ye Long-Wu123,Shi Chong-Yang1,Zhou Bo2

Affiliation:

1. College of Chemistry and Chemical Engineering, Yunnan Normal University

2. Key Laboratory of Chemical Biology of Fujian Province and College of Chemistry and Chemical Engineering, Xiamen University

3. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

Abstract

AbstractThe asymmetric Doyle–Kirmse reaction has become increasingly important in the construction of chiral sulfides, especially for those with quaternary carbon stereocenters. Over the few past decades, a series of catalytic asymmetric approaches have been developed promoted by copper, rhodium, nickel, and other chiral catalysts. Apart from the frequently investigated sulfonium ylides, the enantioselective [2,3]-sigmatropic rearrangement of selenium ylides and iodonium ylides has also been discovered recently. This review summarizes recent advances in the asymmetric Doyle–Kirmse reaction according to the patterns of chirality induction. The synthetic methods for rearranged products, reaction mechanisms and applications are discussed in this review.1 Introduction2 Asymmetric Doyle–Kirmse Reaction Controlled by Chiral Free Ylides3 Asymmetric Doyle–Kirmse Reaction Controlled by Chiral Metal-Bound Ylides4 Conclusion and Outlook

Funder

National Natural Science Foundation of China

Yunnan Normal University

Applied Basic Research Foundation of Yunnan Province

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

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