Boranophosphate diesters as stable synthetic analogues of 1-O- glycosylphosphates

Davide Prosperi; Luigi Panza; Laura Poletti; Luigi Lay

doi:10.1016/S0040-4020(00)00386-0

Boranophosphate diesters as stable synthetic analogues of 1-O- glycosylphosphates

Davide Prosperi, Luigi Panza, Laura Poletti, Luigi Lay

Department of Pharmaceutical Sciences

Research output: Contribution to journal › Article › peer-review

Abstract

Different 1-O-glycosylboranophosphate diesters were synthesised as stable analogues of 1-O-glycosylphosphates, using a one-pot procedure based on the anomeric H-phosphonate of 2,3,4-tri-O-benzyl-α-L-rhamnopyranose as a common precursor. (C) 2000 Elsevier Science Ltd.

Original language	English
Pages (from-to)	4811-4815
Number of pages	5
Journal	Tetrahedron
Volume	56
Issue number	27
DOIs	https://doi.org/10.1016/S0040-4020(00)00386-0
Publication status	Published - 30 Jun 2000

Keywords

Borinating agents
Glycosidic linkage
Phosphodiester bridge

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10.1016/S0040-4020(00)00386-0

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title = "Boranophosphate diesters as stable synthetic analogues of 1-O- glycosylphosphates",

abstract = "Different 1-O-glycosylboranophosphate diesters were synthesised as stable analogues of 1-O-glycosylphosphates, using a one-pot procedure based on the anomeric H-phosphonate of 2,3,4-tri-O-benzyl-α-L-rhamnopyranose as a common precursor. (C) 2000 Elsevier Science Ltd.",

keywords = "Borinating agents, Glycosidic linkage, Phosphodiester bridge",

author = "Davide Prosperi and Luigi Panza and Laura Poletti and Luigi Lay",

note = "Funding Information: We gratefully acknowledge financial support from MURST and CNR, Centro di Studio sulle Sostanze Organiche Naturali.",

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doi = "10.1016/S0040-4020(00)00386-0",

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T1 - Boranophosphate diesters as stable synthetic analogues of 1-O- glycosylphosphates

AU - Prosperi, Davide

AU - Panza, Luigi

AU - Poletti, Laura

AU - Lay, Luigi

N1 - Funding Information: We gratefully acknowledge financial support from MURST and CNR, Centro di Studio sulle Sostanze Organiche Naturali.

PY - 2000/6/30

Y1 - 2000/6/30

N2 - Different 1-O-glycosylboranophosphate diesters were synthesised as stable analogues of 1-O-glycosylphosphates, using a one-pot procedure based on the anomeric H-phosphonate of 2,3,4-tri-O-benzyl-α-L-rhamnopyranose as a common precursor. (C) 2000 Elsevier Science Ltd.

AB - Different 1-O-glycosylboranophosphate diesters were synthesised as stable analogues of 1-O-glycosylphosphates, using a one-pot procedure based on the anomeric H-phosphonate of 2,3,4-tri-O-benzyl-α-L-rhamnopyranose as a common precursor. (C) 2000 Elsevier Science Ltd.

KW - Borinating agents

KW - Glycosidic linkage

KW - Phosphodiester bridge

UR - https://www.scopus.com/pages/publications/0034733632

U2 - 10.1016/S0040-4020(00)00386-0

DO - 10.1016/S0040-4020(00)00386-0

M3 - Article

SN - 0040-4020

VL - 56

SP - 4811

EP - 4815

JO - Tetrahedron

JF - Tetrahedron

IS - 27

ER -

Boranophosphate diesters as stable synthetic analogues of 1-O- glycosylphosphates

Abstract

Keywords

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