A CONVENIENT SYNTHESIS OF (2R)-1-AMINO-1-DEOXY-1-PHOSPHINYLGLYCEROLS

被引:22
作者
HANAYA, T
MIYOSHI, A
NOGUCHI, A
KAWAMOTO, H
ARMOUR, MA
HOGG, AM
YAMAMOTO, H
机构
[1] OKAYAMA UNIV, FAC SCI, DEPT CHEM, OKAYAMA 700, JAPAN
[2] UNIV ALBERTA, DEPT CHEM, EDMONTON T6G 2G2, ALBERTA, CANADA
关键词
D O I
10.1246/bcsj.63.3590
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
2,3-O-Isopropylidene-D-glyceraldehyde reacts with dimethylphosphine oxide in the presence of triethylamine to give separable (1S,2R)- and (1R,2R)-l-dimethylphosphinylglycerol (65:35), from which the (1R) and (1S) title compounds are respectively derived via 1-O-mesyl and 1-azido derivatives. The corresponding 1-dimethoxyphosphinylglycerols are similarly prepared. Structural and conformational assignments of these products are made on the basis of the H-1 NMR data and [alpha]D values.
引用
收藏
页码:3590 / 3594
页数:5
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