作者:Giuseppe Guanti、Luca Banfi、Maria Teresa Zannetti
DOI:10.1016/s0040-4039(00)00326-9
日期:2000.4
racemic β-hydroxyaldehydes bearing a phosphonate group in the ω-position were synthesised and allowed to react with dihydroxyacetone phosphate (DHAP) via an enzymatic aldol addition catalysed by fructose 1,6-bisphosphate aldolase (FruA). After enzymatic dephosphorylation, a set of unnatural ω-phosphonic deoxysugars was obtained.
合成了一系列在ω-位带有膦酸酯基的同源外消旋β-羟醛,并通过果糖1,6-双磷酸醛缩酶(FruA)催化的醛醇加成反应,使其与磷酸二羟基丙酮(DHAP)反应。酶促脱磷酸作用后,获得了一组非天然的ω-膦酸脱氧糖。