Organomanganese (II) reagents XII: An efficient one-pot preparation of unsymmetrical secondary or tertiary alcohols
作者:G Cahiez、J Rivas-Enterrios、H Granger-Veyron
DOI:10.1016/s0040-4039(00)84973-4
日期:1986.1
Various unsymmetrical secondary or tertiary alcohols have been prepared in high yields by an efficient one-pot procedure involving the acylation of an organomanganese reagent by an acyl chloride and addition to the ketone formed of various organometallic compounds (RLi, RmgX, LiAlH4, NaBH4. The complexation of the intermediate ketone by the metallic salts present in the reaction mixture allows to perform
已经通过有效的一锅法高产率地制备了各种不对称的仲或叔醇,该一锅法包括通过酰氯对有机锰试剂进行酰化反应,并将其添加到由各种有机金属化合物(RLi,RmgX,LiAlH 4,NaBH 4。中间酮与反应混合物中存在的金属盐的络合使得可以在异常温和的条件下(0至20°C)执行1-2加成步骤。