Journal
ORGANIC LETTERS
Volume 20, Issue 4, Pages 1183-1186Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b00065
Keywords
-
Categories
Funding
- Indian Institute of Technology Madras [CHY/16-17/840/RFIR/ANBA]
- CSIR, New Delhi
Ask authors/readers for more resources
An efficient acid-mediated oxythiolation of o-vinylanilides has been accomplished, employing N-(arylthio)-succinimide as an electrophilic arylthiolating reagent for the synthesis of various arylthio tethered benzoxazine derivatives in good to excellent yield. The important features of this method include wide functional group tolerance, quick reaction time, absence of metal or additive, and excellent substrates scope. The developed method was also successfully extended to the oxyselenation of o-vinylanilides in the absence of acid promoter.
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