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出 处:《Chinese Journal of Chemistry》2002年第12期1591-1597,1464,共0页中国化学(英文版)
基 金:theNationalNaturalScienceFoundationofChina (No. 2 986 2 0 0 4),theScienceandTechnologyDevelopmentProgramFoundationofJilinProvince (No.2 0 0 10 5 0 5)andtheYouthFoundationofNortheastNormalUniversity (No.111379)
摘 要:A facile route to 2-benzylthio-5-phenyl-3,4-disubstituted thiophenes was described. Catalyzed by sodium hydroxide, the title compounds were synthesized in moderate to good yields simply from the intramolecular aldol type condensation of α-oxo ketene dibenzylthioacetals. The chemical selectivity for this annulation reaction was studied and discussed.A facile route to 2-benzylthio-5-phenyl-3,4-disubstituted thiophenes was described. Catalyzed by sodium hydroxide, the title compounds were synthesized in moderate to good yields simply from the intramolecular aldol type condensation of α-oxo ketene dibenzylthioacetals. The chemical selectivity for this annulation reaction was studied and discussed.
关 键 词:α-oxo ketene dithioacetals α-oxo ketene dibenzylthioacetals multisubstituted thiophenes intramolecular aldol type condensation
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