期刊
CHEMICAL COMMUNICATIONS
卷 -, 期 18, 页码 2399-2401出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b502134k
关键词
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Vinylic hydrogens at the β-position of enones were effectively substituted with alkyl groups in a one-pot procedure to afford β-alkyl enones in good to high isolated yields by conjugate addition of higher-order dialkyl cyanocuprates to enones, followed by a reaction with N-tert-butylbenzenesulfinimidoyl chloride at -78 ° C.
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