(Alkoxyallyl)sulfones as enal and enone β-anion equivalents. Synthesis of mono-, di- and trisubtituted furans
摘要:
Treatment of variously-substituted (alkoxyallyl)sulfones 1, 7-9 with strong base followed by aldehydes gives alcohol adducts 5. These may be converted into a wide range of substituted furans 6 by exposure to acid, or to silica gel in dichloromethane containing sulfuric acid in some cases. Copyright (C) 1996 Elsevier Science Ltd
Diastereoselective Synthesis of α-Oxyaminesvia Gold-, Silver- and Copper-Catalyzed, Three-Component Couplings of α-Oxyaldehydes, Alkynes, and Amines in Water
作者:Baosheng Huang、Xiaoquan Yao、Chao-Jun Li
DOI:10.1002/adsc.200606118
日期:2006.8
The three-componentcouplings of α-oxyaldehydes, alkynes, and amines in water were investigated by using gold, silver and copper catalysts. Gold(I) was found to be the most effective catalyst in this reaction to afford propargylamines in good yields and moderate diastereoselectivities. On the other hand, silver catalysts show the best catalytic activities on non-coordinating α-alkyl-substituted aldehydes