Synthesis of Acetylated Ranunculin Diastereoisomers and δ-Glucosyloxy-γ-Oxo Esters from α or β Glucosylmethylfurfural

Synthesis of Acetylated Ranunculin Diastereoisomers and δ-Glucosyloxy-γ-Oxo Esters from α or β Glucosylmethylfurfural

The α and β acetylated (5-formyl-2-furyl)methyl-D-glucopyranosides were synthesized and converted into acetylated ranunculin diastereoisomers and δ-glucosyloxy-γ-oxo esters.

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Bibliographic Details
Published in:Journal of carbohydrate chemistry Vol. 24; no. 1; pp. 55 - 71
Main Authors: Cottier, Louis, Descotes, Gérard, Soro, Yaya
Format: Journal Article
Language:English
Published: Taylor & Francis Group 01-01-2005
Subjects:
Furanic compounds
Glycosylation
Photooxygenation
Synthesis
Online Access:Get full text
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Description
Summary:The α and β acetylated (5-formyl-2-furyl)methyl-D-glucopyranosides were synthesized and converted into acetylated ranunculin diastereoisomers and δ-glucosyloxy-γ-oxo esters.
ISSN:0732-8303
1532-2327
DOI:10.1081/CAR-200049688