The C-glycosidic analogue of α-L-rhamnose 1-phosphate has been stereoselectively synthesised reacting 2,3,4-tri-O-benzyl-L-rhamnopyranose with tetraethyl methylenediphosphonate and sodium hydride in diglyme, and then deprotecting with iodotrimethylsilane.

Cipolla, L., LA FERLA, B., Nicotra, F., & Panza, L. (1997). Easy and Stereoselective Synthesis of the Phosphono Analogue of a-L-Rhamnose 1-phosphate. TETRAHEDRON LETTERS, 5567-5568.

Easy and Stereoselective Synthesis of the Phosphono Analogue of a-L-Rhamnose 1-phosphate

CIPOLLA, LAURA FRANCESCA;LA FERLA, BARBARA;NICOTRA, FRANCESCO;
1997

Abstract

The C-glycosidic analogue of α-L-rhamnose 1-phosphate has been stereoselectively synthesised reacting 2,3,4-tri-O-benzyl-L-rhamnopyranose with tetraethyl methylenediphosphonate and sodium hydride in diglyme, and then deprotecting with iodotrimethylsilane.
Articolo in rivista - Articolo scientifico
carbohydrate
English
5567
5568
2
Cipolla, L., LA FERLA, B., Nicotra, F., & Panza, L. (1997). Easy and Stereoselective Synthesis of the Phosphono Analogue of a-L-Rhamnose 1-phosphate. TETRAHEDRON LETTERS, 5567-5568.
Cipolla, L; LA FERLA, B; Nicotra, F; Panza, L
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/17010
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