Cs2CO3-Promoted Michael Addition-[2,3]-Sigmatropic Rearrangement Domino Reaction: Facile Synthesis of a 3-Substituted Indoles Bearing a Homoallyl Sulfide Moiety-Reference-Cited by-同舟云学术

Cs2CO3-Promoted Michael Addition-[2,3]-Sigmatropic Rearrangement Domino Reaction: Facile Synthesis of a 3-Substituted Indoles Bearing a Homoallyl Sulfide Moiety

Published:2016-09-22 Issue:11 Volume:5 Page:1309-1313
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Du Yanlong¹,Yu Aimin¹,Zhang Youquan¹,Jia Jiru¹,Meng Xiangtai¹

Affiliation:

1. Tianjin Key Laboratory of Organic Solar Cells and Photochemical Conversion; School of Chemistry & Chemical Engineering; Tianjin University of Technology; Tianjin 300384 P. R. China

Publisher

Wiley

Subject

Organic Chemistry

Reference55 articles.

1. A Sulfur Ylides-Mediated Domino Benzannulation Strategy to Construct Biaryls, Alkenylated and Alkynylated Benzene Derivatives

2. Tandem Michael Addition/Ylide Epoxidation for the Synthesis of Highly Functionalized Cyclohexadiene Epoxide Derivatives

3. Highly Functionalized 4-Alkylidenebicyclo[3.1.0]hex-2-enes by Tandem Michael Addition and Annulation of Electron-Deficient Enynes

4. Domino Reaction for the Chemo- and Stereoselective Synthesis of trans-2,3-Dihydrobenzofurans from N-Thiophosphinyl Imines and Sulfur Ylides

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