119646-32-1Relevant academic research and scientific papers
B(C6F5)3 as a highly effective catalyst for the phosphoryl transfer reaction
Xue, Weihua,Zhang, Lifen
, p. 1797 - 1800 (2012/10/29)
The phosphoryl transfer reactions of diphenyl chlorophosphate with a wide range of alcohols were catalyzed by tris(pentafluorophenyl)boron [B(C 6F5)3], giving the corresponding phosphate esters in excellent yields. This me
Autocleavage of O-isopropylidene protected O-phosphono- and O-thionophosphono esters of sugars
Postel, Denis,Ronco, Gino,Villa, Pierre
, p. 171 - 192 (2007/10/03)
Phosphorylation of D-glucose, D-galactose, D-fructose, glycerol and xylitol acetals with diethoxy-or diphenoxy(thiono)phosphoryl chloride gave the corresponding esters. A novel method of partially and fully deprotecting these compounds, which we have call
Synthesis and Transformation of Sugar Phosphates
Bogusiak, J.,Szeja, W.
, p. 2181 - 2186 (2007/10/02)
Sugar diphenyl phosphates can be conveniently prepared by the treatment of monosaccharides with diphenylphosphorochloridate under phase-transfer conditions. Key words: synthesis, phosphorylation, sugar phosphates, catalytic two-phase system, thiosugars
