115221-03-9Relevant academic research and scientific papers
SYNTHESE DE PHOSPHORAMIDATES DE 2-DESOXY-2-IODOGLYCOSYLES
Lafont, Dominique,Descotes, Gerard
, p. 195 - 210 (2007/10/02)
Addition of iodoazide to acetylated, benzylated, and methoxymethylated glycals yielded 2-deoxy-2-iodoglycosyl azides with 1,2-trans configuration.Stereoselectivity of the reaction favored the manno and talo configurations starting from D-glucal and D-galactal, respectively.With D-xylal derivatives, the stereoselectivity depended on the nature of the substituents.The Staudinger reaction of 2-deoxy-2-iodoglycosyl azides with trimethylphosphite led to the corresponding 2-deoxy-iodoglycosyl phosphoramidates in high yield.
