Journal
CHEMICAL COMMUNICATIONS
Volume 58, Issue 61, Pages 8508-8511Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cc02892a
Keywords
-
Categories
Ask authors/readers for more resources
A new photoredox approach has been reported for the one-step synthesis of oxazetidines with a free -NH group, using the combined use of alkyne, thiophenol, and azide. The synthesized oxazetidine with the -NH group was found to be stable enough for various late-stage transformations.
A photoredox approach enabling one-step synthesis of oxazetidines with a free -NH group via the combined use of alkyne, thiophenol, and azide has been reported. The synthesized oxazetidine with the free -NH group was stable enough for various late-stage transformations such as methylation, acetylation, tosylation, and ring-opening reaction to afford synthetically useful alpha-aminoketones.
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