4.0 Article

Preparation of methyl 6-O-p-nitrobenzoyl-beta-D-glucoside

Journal

JOURNAL OF CARBOHYDRATE CHEMISTRY
Volume 27, Issue 3, Pages 188-199

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/07328300802071245

Keywords

nonreducing end; NBS; cyclic acetals; oxidation; nitrobenzoyl

Ask authors/readers for more resources

Methyl 6-O-p-nitrobenzoyl-beta-D-glucoside was synthesized by reacting methyl 4,6-O-p-nitrobenzylidine-beta-D-glucoside with N-bromosuccinimide (NBS). First, methyl beta-D-glucoside was converted into methyl 4,6-O-p-nitrobenzylidine-beta-D-glucoside with p-nitrobenzaldehyde. Later, methyl 4,6-O-p-nitrobenzylidine-beta-D-glucoside was opened oxidatively with NBS to give methyl 6-O-p-nitrobenzoyl-beta-D-glucoside.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.0
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available