From methyl d-glucopyranoside to methyl d-allopyranoside via the Mitsunobu reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference13 articles.
1. Large-scale preparation of D-allose: observations on the stereoselectivity of the reduction of 1,2:5,6-di-O-isopropylidene-α-D-ribo-hexofuranos-3-ulose hydrate
2. Synthesis of the methyl D-allopyranosides and of D-allose from 1,2:5,6-DI-O-isopropylidine-3-O-p-tolylsulfonyl-α-D-glucofuranose
3. The Mitsunobu reaction on methyl glycosides as alcohol component
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1. Site-Selective Functionalization of Hydroxyl Groups in Carbohydrate Derivatives;Chemical Reviews;2018-12-03
2. Regioselective Benzoylation of Diols and Carbohydrates by Catalytic Amounts of Organobase;Molecules;2016-05-17
3. Regioselective modification of unprotected glycosides;Chemical Communications;2016
4. Studies on the stereoselective synthesis of a protected α-d-Gal-(1→2)-d-Glc fragment;Carbohydrate Research;2011-07
5. ChemInform Abstract: From Methyl D-Glucopyranoside to Methyl D-Allopyranoside via the Mitsunobu Reaction.;ChemInform;2010-06-10
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