We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Cs<sub>2</sub>CO<sub>3</sub>-Promoted Michael Addition-[2,3]-Sigmatropic Rearrangement Domino Reaction: Facile Synthesis of a 3-Substituted Indoles Bearing a Homoallyl Sulfide Moiety.
- Authors
Du, Yanlong; Yu, Aimin; Zhang, Youquan; Jia, Jiru; MENg, Xiangtai
- 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.
- Subjects
SULFIDE crystals; SULFIDE synthesis; SCISSION (Chemistry)
- Publication
Asian Journal of Organic Chemistry, 2016, Vol 5, Issue 11, p1309
- ISSN
2193-5807
- Publication type
Article
- DOI
10.1002/ajoc.201600343