Fine Control of Regioselectivity in the Reduction of NAD<sup>+</sup>Analogues by Ketene Silyl Acetals
作者:Shunichi Fukuzumi、Morifumi Fujita、Souta Noura、Junzo Otera
DOI:10.1246/cl.1993.1025
日期:1993.6
Various NAD+ analogues are reduced regioselectively by ketene silyl acetals to afford the corresponding 2-, 6-, or 4-alkylated NADH analogues. The regioselectivity of the 1,2- (or 1,6-) vs. 1,4-reduction is finely controlled by the β-methyl-substitution of ketene silyl acetals, the position of methyl-substitution of NAD+ analogues, and the addition of Et4NCl or Bu4NF.
各种 NAD+ 类似物通过乙缩酮硅烷进行区域选择性还原,从而得到相应的 2-、6- 或 4-烷基化 NADH 类似物。1,2-(或 1,6-)与 1,4-还原的区域选择性受烯甲硅基乙醛的 β-甲基取代、NAD+ 类似物的甲基取代位置以及 Et4NCl 或 Bu4NF 的添加等因素的严格控制。