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

Dipartimento di Scienze del Farmaco

Risultato della ricerca: Contributo su rivista › Articolo in rivista

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.

Lingua originale	Inglese
pagine (da-a)	5567-5567
Numero di pagine	5567
Rivista	Tetrahedron Letters
Volume	38
Stato di pubblicazione	Pubblicato - 1997

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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.",

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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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