作者:L Domon、F Vogeleisen、D Uguen
DOI:10.1016/0040-4039(96)00417-0
日期:1996.4
Enzyme-catalysed acetylation of either syn,syn- or anti,anti-2,4-dimethyl-1,3,5-pentanetriol, easily obtained from a mixture of diastereomeric 3-hydroxy-2,4-dimethylglutaric acids, proceeds stereoselectively with preferential attack of the hydromethyl group linked to the R carbon atom of the starting triol, hence providing synthons useful for preparing compounds of the polypropionic pool.
顺式,顺式或反式,反式,2,4-二甲基-1,3,5-戊烷三醇的酶催化乙酰化反应,可轻松地从非对映异构体3-羟基-2,4-二甲基戊二酸的混合物中获得,并进行立体选择性具有与起始三醇的R碳原子相连的氢甲基的优先攻击,因此提供了可用于制备聚丙烯酸酯池化合物的合成子。