作者:Berry M. Trost、Maria S. Rodriguez
DOI:10.1016/s0040-4039(00)61256-x
日期:1992.8
A six step synthesis of S-(−)-ipsenol, a constituent of the sex pheromone of the bark beetle, from lactic acid employs an asymmetric aldol condensation and a novel molybdenum catalyzed elimination of an allyl ester as key steps.
由乳酸的六步合成S-(-)-艾普森醇(树皮甲虫性信息素的组成部分)采用不对称的羟醛缩合和新颖的钼催化的烯丙基酯消除作为关键步骤。