作者:Solveig Roussel、Thierry Billard、Bernard R. Langlois、Laurent Saint-James
DOI:10.1002/chem.200400777
日期:2005.1.21
Various trifluoroacetamides and trifluoromethanesulfinamides, derived from chiral silylated amino alcohols, have been synthesized with the goal of achieving enantioselective nucleophilic trifluoromethylation. The best results were obtained with (R)-phenylglycinol derivatives, but the ee values did not exceed 30 %.
为了达到对映选择性亲核三氟甲基化的目的,已经合成了衍生自手性甲硅烷基化氨基醇的各种三氟乙酰胺和三氟甲亚磺酰胺。(R)-苯基甘氨醇衍生物获得了最佳结果,但ee值不超过30%。