期刊
CHEMICAL COMMUNICATIONS
卷 -, 期 38, 页码 3921-3923出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b710393j
关键词
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The first organocatalytic anti-Michael'' reaction of cyclic-beta-ketoesters to unsaturated double bonds is described in a highly asymmetric version leading to the synthesis of alpha,alpha'-di-substituted branched double bonds as optically active Baylis-Hillman-like adducts.
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