Easy and stereoselective synthesis of the phosphono analogue of α-L-rhamnose 1-phosphate

Laura Cipolla; Barbara La Ferla; Francesco Nicotra; Luigi Panza

doi:10.1016/S0040-4039(97)01245-8

Easy and stereoselective synthesis of the phosphono analogue of α-L-rhamnose 1-phosphate

Laura Cipolla
, Barbara La Ferla
, Francesco Nicotra
, Luigi Panza

Risultato della ricerca: Contributo su rivista › Articolo in rivista › peer review

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)	5567-5568
Numero di pagine	2
Rivista	Tetrahedron Letters
Volume	38
Numero di pubblicazione	31
DOI	https://doi.org/10.1016/S0040-4039(97)01245-8
Stato di pubblicazione	Pubblicato - 4 ago 1997
Pubblicato esternamente	Sì

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10.1016/S0040-4039(97)01245-8

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title = "Easy and stereoselective synthesis of the phosphono analogue of α-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 = "Laura Cipolla and \{La Ferla\}, Barbara and Francesco Nicotra and Luigi Panza",

year = "1997",

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T1 - Easy and stereoselective synthesis of the phosphono analogue of α-L-rhamnose 1-phosphate

AU - Cipolla, Laura

AU - La Ferla, Barbara

AU - Nicotra, Francesco

AU - Panza, Luigi

PY - 1997/8/4

Y1 - 1997/8/4

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://www.scopus.com/pages/publications/0030792965

U2 - 10.1016/S0040-4039(97)01245-8

DO - 10.1016/S0040-4039(97)01245-8

M3 - Article

SN - 0040-4039

VL - 38

SP - 5567

EP - 5568

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 31

ER -

Easy and stereoselective synthesis of the phosphono analogue of α-L-rhamnose 1-phosphate

Abstract

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