Synthesis of phosphono analogues of dihydroxyacetone phosphate and glyceraldehyde 3-phosphate
作者:Patrick Page、Casimir Blonski、Jacques Périé
DOI:10.1016/s0968-0896(99)00065-6
日期:1999.7
routes of six phosphono analogues of dihydroxyacetone phosphate and five phosphono analogues of glyceraldehyde 3-phosphate through alpha-, beta- and gamma-hydroxyphosphonate esters precursors containing a protected carbonyl group. In some situations, depending on the sequence used for the deprotection of the phosphonate and carbonyl groups, the aldol/ketol rearrangement allowed the synthesis of either
本文介绍了六羟基二磷酸丙酮的膦酰基类似物和3-磷酸甘油醛的五个膦酰基类似物通过含有保护的羰基的α-,β-和γ-羟基膦酸酯前体的合成途径。在某些情况下,取决于用于膦酸酯和羰基的脱保护的序列,羟醛/酮醇重排允许由相同的前体合成磷酸二羟基丙酮或3-磷酸甘油醛的类似物。所有这些类似物均作为活性位点探针和糖酵解酶(例如果糖1,6-二磷酸醛缩酶)(EC 4.1.2.13)的潜在底物都受到关注。