Completely stereospecific 1,2-migration of alkyl groups in Et2AlCl promoted pinacol-type rearrangement
作者:Gen-ichi Tsuchihashi、Katsuhiko Tomooka、Keisuke Suzuki
DOI:10.1016/s0040-4039(01)81409-x
日期:1984.1
Completely stereospecific 1,2-migration of alkyl groups was achieved in Et2AlCl promoted pinacol-type rearrangement of chiral β-mesyloxy alcohols to give optically pure α-alkyl ketones including both enantiomers of 4-methyl-3-hexanone, an alarm pheromone of ant.
在Et 2 AlCl促进的手性β-甲磺酰氧基醇的频哪醇型重排中实现了烷基的完全立体定向的1,2-迁移,从而得到了光学纯的α-烷基酮,包括4-甲基-3-己酮(警报信息素)的两种对映体。的蚂蚁。