Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 21, Issue 42, Pages 8528-8534Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ob01473h
Keywords
-
Categories
Ask authors/readers for more resources
In this study, various nitrogen nucleophiles were easily added to in situ-generated 1-(trifluoromethyl)-2-(phenylthio)ethyne to afford the corresponding trifluoromethyl enamines in good-to-high yields and with high regio- and stereocontrol under very mild conditions.
Various nitrogen nucleophiles were easily added to in situ-generated 1-(trifluoromethyl)-2-(phenylthio)ethyne to afford the corresponding trifluoromethyl enamines in good-to-high yields and with high regio- and stereocontrol under very mild conditions.
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