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Chemoselective Bromodecarboxylation ofα-Carboxy-α-cinnamoyl Ketene Cyclic Dithioacetals 被引量:4
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作者 WANG Mang XU Xian-xiu +1 位作者 LIU Qun YANG Xiao-xia 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2005年第5期626-629,共4页
α-Oxoketene dithioacetals( compound 1 ) are versatile synthons for organic synthesis due to their specially structural characteristic, that is, the masked ketene is conjugated with the convertible carbonyl in their... α-Oxoketene dithioacetals( compound 1 ) are versatile synthons for organic synthesis due to their specially structural characteristic, that is, the masked ketene is conjugated with the convertible carbonyl in their molecules. Although there have been numerous reports covering the reactions in which they have been taken as 1,3-electrophiles, the reaction at the α-carbon atom of α-oxoketene dithioacetals has seldom been investigated. Junjappa and co-workers found the α- bromination of compound 2 in the presence of NBS led to α-aroyl-α-bromo ketenedithioacetals. However, the flexibility of the functional groups at the α-carbon atom of compound 2 are still limited. 展开更多
关键词 CHEMOSELECTIVE bromodecarboxylation α-Carboxy-α-cinnamoyl ketene cyclic dithioacetal
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