期刊
ORGANIC LETTERS
卷 17, 期 12, 页码 2944-2947出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b01221
关键词
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资金
- IISc
- DST (SERB), New-Delhi
- CSIR
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.
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