Journal
ORGANIC LETTERS
Volume 17, Issue 12, Pages 2944-2947Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b01221
Keywords
-
Categories
Funding
- IISc
- DST (SERB), New-Delhi
- CSIR
Ask authors/readers for more resources
Sulfenylation of beta-diketones is challenging as beta-diketones undergo deacylation after sulfenylation in the reaction medium. The sulfenylation of beta-diketones without deacylation under metal-free conditions at ambient temperature via a cross dehydrogenative coupling (CDC) strategy is reported. The resultant products can be further manipulated to form alpha,alpha-disubstituted beta-diketones and pyrazoles.
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