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                                       Details for article 8 of 252 found articles
 
 
  Alkylating γ-Lactone-Opening: A Short Synthesis of Benzyl 3-O-Benzyl-1,2-O-isopropylidene-α-D-glucofuranuronate
 
 
Title: Alkylating γ-Lactone-Opening: A Short Synthesis of Benzyl 3-O-Benzyl-1,2-O-isopropylidene-α-D-glucofuranuronate
Author: Wessel, Hans Peter
Appeared in: Journal of carbohydrate chemistry
Paging: Volume 8 (1989) nr. 3 pages 443-455
Year: 1989-07-01
Contents: γ-Lactones were reacted with barium oxide/barium hydroxide/benzyl bromide in dimethylformamide to result in simultaneous benzylation of the γ-hydroxyl group and esterification of the carboxylic acid. A suitable protecting group for an α-hydroxyl function proved to be the tetrahydropyranyl group. The title compound was thus obtained in four steps from D-glucurono-6, 3-lactone.
Publisher: Taylor & Francis
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 8 of 252 found articles
 
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