Rh(II)-catalyzed [2,3]-sigmatropic rearrangement of sulfur ylides derived from N-tosylhydrazones and sulfides-Reference-Cited by-同舟云学术

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Rh(II)-catalyzed [2,3]-sigmatropic rearrangement of sulfur ylides derived from N-tosylhydrazones and sulfides

Published:2012-07 Issue:26 Volume:68 Page:5234-5240
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Li Yuye,Huang Zhongxing,Wu Xinhu,Xu Peng-Fei,Jin Jing,Zhang Yan,Wang Jianbo

Funder

National Natural Science Foundation of China

Ministry of Education - Singapore

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference57 articles.

1. For selected reviews, see:

2. Sulfur-mediated ring expansions in total synthesis

3. Asymmetric Ylide Reactions: Epoxidation, Cyclopropanation, Aziridination, Olefination, and Rearrangement

4. Perturbation of rearrangement courses by cyclohepta-amylose

5. Sulfur Ylides;Trost,1975

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1. Rh(II)-Catalyzed Si–H Insertion with Nosyl-hydrazone-Protected Aryl Donor Diazo Compounds;ACS Omega;2023-10-06

2. Rh-Catalyzed [2,3]-Sigmatropic Rearrangement of Alkynyl Carbenes with Allyl Sulfides to Access Sulfide-Substituted 1,5-Enynes;The Journal of Organic Chemistry;2023-06-30

3. Rh(II) catalyzed efficient sigmatropic rearrangement reaction of pyridotriazoles and sulfides;Green Synthesis and Catalysis;2023-04

4. Nitrogen- and Sulfur-Based Stevens and Related Rearrangements;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023

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