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

L. CIPOLLA; FERLA B. LA; F. NICOTRA; Luigi PANZA

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

L. CIPOLLA, FERLA B. LA, F. NICOTRA, Luigi PANZA

Department of Pharmaceutical Sciences

Research output: Contribution to journal › Article

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.

Original language	English
Pages (from-to)	5567-5567
Number of pages	5567
Journal	Tetrahedron Letters
Volume	38
Publication status	Published - 1997

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@article{f7c84a6f655049d2b31f83b78dce68ea,

title = "Easy and Stereoselective Synthesis of the Phosphono Analogue of a-L-Rhamnose 1-Phosphate",

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.",

author = "L. CIPOLLA and LA, {FERLA B.} and F. NICOTRA and Luigi PANZA",

year = "1997",

language = "English",

volume = "38",

pages = "5567--5567",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd.",

}

TY - JOUR

T1 - Easy and Stereoselective Synthesis of the Phosphono Analogue of a-L-Rhamnose 1-Phosphate

AU - CIPOLLA, L.

AU - LA, FERLA B.

AU - NICOTRA, F.

AU - PANZA, Luigi

PY - 1997

Y1 - 1997

N2 - 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.

AB - 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.

UR - https://iris.uniupo.it/handle/11579/7376

M3 - Article

SN - 0040-4039

VL - 38

SP - 5567

EP - 5567

JO - Tetrahedron Letters

JF - Tetrahedron Letters

ER -

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

Abstract

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