作者:Suk-Ku Kang、Hyun-Sung Cho
DOI:10.1016/s0040-4039(00)92630-3
日期:1991.1
(S)-3-Formyloxyaldehydes, chiral synthons for natural product synthesis were synthesized via highly stereoselective hydrogenation of the unsaturated furanose ring system derived from D-glucose or D-xylose. Alternatively, (R)-3-formyloxyaldehydes were prepared via deoxygenation of 3-hydroxyfuranoses derived from D-glucose or D-xylose.
通过高度立体选择性氢化衍生自D-葡萄糖或D-木糖的不饱和呋喃糖环系统合成了用于天然产物合成的(S)-3-Formyloxyaldehydes,手性合成子。或者,通过使衍生自D-葡萄糖或D-木糖的3-羟基呋喃糖酶脱氧制备(R)-3-甲酰氧基醛。