Journal
CHEMICAL COMMUNICATIONS
Volume 56, Issue 42, Pages 5649-5652Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc00016g
Keywords
-
Categories
Funding
- DST-SERB, New Delhi, India [EMR/2016/003677]
- Council of Scientific & Industrial Research (CSIR)
Ask authors/readers for more resources
An efficient rhodium catalyzed Sommelet-Hauser type rearrangement of sulfur ylides derived from alpha-thioesters and N-sulfonyl-1,2,3-triazoles has been successfully accomplished for the synthesis of various functionalized enamides. The developed reaction involves the unprecedented [2,3]-sigmatropic rearrangement of sulfur ylides with the imine motif. Importantly, the method works well with various substituted alpha-thioesters/-amides/-ketones and substituted N-sulfonyl-1,2,3-triazoles and allows the synthesis of diverse enamide derivatives in good to excellent yields. The reaction was also successfully extended to the one-pot synthesis of enamides from terminal alkynes.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available