期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 73, 期 11, 页码 4241-4244出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo800428b
关键词
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A series of 3,3-diarylacrylonitriles were synthesized stercoselectively as tubulin polymerization inhibitors for potential use in cancer chemotherapy. This synthetic route features stannylcupration and palladium-catalyzed Stille cross-coupling chemistry, allowing both E and Z isomers of 3,3-diarylacrylonitriles to be prepared in a very short sequence of reactions.
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