Synthesis of transition state inhibitors for N-riboside hydrolases and transferases
作者:Richard H Furneaux、Gerrit Limberg、Peter C Tyler、Vern L Schramm
DOI:10.1016/s0040-4020(96)01172-6
日期:1997.2
A number of 1,4-dideoxy-1,4-imino-1-(S)-(substituted phenyl)-d-ribitols bearing aromatic OH, NH2, NO2, CO2H and halogeno moieties, and a 3-pyridyl analogue have been synthesized. The key step is the condensation of aryllithium or aryl Grignard reagents with the imine 3; derived from the protected 1,4-dideoxy-1,4-imino-d-ribitol 4.
许多带有芳族OH,NH 2,NO 2,CO 2 H和卤素部分的1,4-二脱氧-1,4-亚氨基-1-(S)-(取代的苯基)-d-核糖醇,以及3-吡啶类似物已经合成。关键步骤是芳基锂或芳基格氏试剂与亚胺3的缩合。衍生自受保护的1,4-二脱氧-1,4-亚氨基-d-核糖醇4。