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-alpha-L-rhamnopyranose as a common precursor. (C) 2000 Elsevier Science Ltd. All rights reserved.

Boranophosphate diesters as stable synthetic analogues of 1-O-glycosylphosphates / D. Prosperi, L. Panza, L. Poletti, L. Lay. - In: TETRAHEDRON. - ISSN 0040-4020. - 56:27(2000), pp. 4811-4815.

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

L. Poletti
Penultimo
;
L. Lay
2000

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-alpha-L-rhamnopyranose as a common precursor. (C) 2000 Elsevier Science Ltd. All rights reserved.
Borinating agents; Glycosidic linkage; Phosphodiester bridge
Settore CHIM/06 - Chimica Organica
2000
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/188286
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