期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 17, 页码 6419-6422出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja401867b
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资金
- National Institutes of Health [R01 GM85235]
The first catalytic, enantioselective carbosulfenylation of alkenes with an aromatic nucleophile is described, using a BINAM-based selenophosphoramide catalyst. E-Alkyl- and aryl-substituted alkenes afforded tetrahydronaphthalenes with complete diastereospecificity, and generally high enantiomeric ratios.
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