2-(1,3-dithian-2-ylidene)-1-arylethenones 3 Via chemoselective 1,2-addition with methyl,ethyl, phenyl,allyl,and benzyl Grignard reagents afforded the corresponding alcohols(4).Catalyzing by silica gel,the alcohols 4 w...2-(1,3-dithian-2-ylidene)-1-arylethenones 3 Via chemoselective 1,2-addition with methyl,ethyl, phenyl,allyl,and benzyl Grignard reagents afforded the corresponding alcohols(4).Catalyzing by silica gel,the alcohols 4 were converted to the aryl.ketones(5).The entire process represent a demethylation— alkylation reaction of acetophenones.The mechanism of reaction are proposed and the structure requirement for the conversion of the alcohols(4)was discussed.展开更多
文摘2-(1,3-dithian-2-ylidene)-1-arylethenones 3 Via chemoselective 1,2-addition with methyl,ethyl, phenyl,allyl,and benzyl Grignard reagents afforded the corresponding alcohols(4).Catalyzing by silica gel,the alcohols 4 were converted to the aryl.ketones(5).The entire process represent a demethylation— alkylation reaction of acetophenones.The mechanism of reaction are proposed and the structure requirement for the conversion of the alcohols(4)was discussed.