期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 74, 期 11, 页码 4188-4194出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo900347s
关键词
-
资金
- Fonds der Chemischen Industrie
- Deutsche Forschunusgemeinschaft
1-(N,N-Diisopropylcarbamoyloxy)-1-tosyl-alkenes have been developed as an a(2)d(1) synthon via tandem umpolung. Upon addition of Grignard reagents and further quench by carbonyl compounds, this synthon produces alpha,alpha'-branched-alpha'-oxygenated ketones. Strategically, this widely applicable method installs respectively a carbanion unit and a carbonyl unit formally onto the alpha-carbon and the carbonyl center of an aldehyde in one-pot.
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