Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 14-Day Trial for You or Your Team.

Learn More →

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

Cs2CO3‐Promoted Michael Addition‐[2,3]‐Sigmatropic Rearrangement Domino Reaction: Facile... A Cs2CO3‐promoted Michael addition‐[2,3]‐sigmatropic rearrangement domino reaction between arenesulfonylindole and sulfur ylide has been developed. This reaction affords a facile method for the synthesis of 3‐substituted indoles with a homoallyl sulfide moiety. In this domino sequence, two C−C bonds and one C−C bond cleavage were formed. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Asian Journal of Organic Chemistry Wiley

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

Loading next page...
 
/lp/wiley/cs2co3-promoted-michael-addition-2-3-sigmatropic-rearrangement-domino-uWMUqUjJJV

References (45)

Publisher
Wiley
Copyright
© 2016 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
ISSN
2193-5807
eISSN
2193-5815
DOI
10.1002/ajoc.201600343
Publisher site
See Article on Publisher Site

Abstract

A Cs2CO3‐promoted Michael addition‐[2,3]‐sigmatropic rearrangement domino reaction between arenesulfonylindole and sulfur ylide has been developed. This reaction affords a facile method for the synthesis of 3‐substituted indoles with a homoallyl sulfide moiety. In this domino sequence, two C−C bonds and one C−C bond cleavage were formed.

Journal

Asian Journal of Organic ChemistryWiley

Published: Nov 1, 2016

Keywords: ; ; ;

There are no references for this article.