Investigation of Meyer-Schuster Rearrangement Promoted by a Samarium(III) Triflate/N-Fluorobenzenesulfonimide Lewis Acid System-Reference-Cited by-同舟云学术

Investigation of Meyer-Schuster Rearrangement Promoted by a Samarium(III) Triflate/N-Fluorobenzenesulfonimide Lewis Acid System

Published:2016-04-18 Issue:6 Volume:5 Page:755-762
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Du Chuan¹²,Wang Xiaoyu¹²,Jin Shengfei¹²,Shi Hui¹²,Li Yangming¹²,Pang Yadong¹²,Liu Yang¹,Cheng Maosheng¹²,Guo Chun¹,Liu Yongxiang¹²

Affiliation:

1. Key Laboratory of Structure-Based Drug Design and Discovery; Shenyang Pharmaceutical University; Ministry of Education; Shenyang 110016 P. R. China

2. Institute of Drug Research in Medicine Capital of China; Benxi 117000 P. R. China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Liaoning Province of China

Foundation of Liaoning Province Education Administration of China

Ministry of Education

Program for Liaoning Innovative Research Team in University

Publisher

Wiley

Subject

Organic Chemistry

Reference68 articles.

1. Rupe and Meyer-Schuster rearrangements

2. The Meyer–Schuster rearrangement for the synthesis of α,β-unsaturated carbonyl compounds

3. Metal-catalyzed transformations of propargylic alcohols into α,β-unsaturated carbonyl compounds: from the Meyer–Schuster and Rupe rearrangements to redox isomerizations

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