From secondary alcohols to tertiary fluoro substituents: A simple route to hydroxymethyl branched sugars with a fluorine substituent at the branching point.
Schalli, Michael
From secondary alcohols to tertiary fluoro substituents: A simple route to hydroxymethyl branched sugars with a fluorine substituent at the branching point. [electronic resource] - Carbohydrate research Dec 2016 - 11-19 p. digital
Publication Type: Journal Article
1873-426X
10.1016/j.carres.2016.10.013 doi
Alcohols--chemistry
Carbohydrates--chemistry
Fluorides--chemistry
Fluorine--chemistry
Molecular Structure
Oxidation-Reduction
Stereoisomerism
From secondary alcohols to tertiary fluoro substituents: A simple route to hydroxymethyl branched sugars with a fluorine substituent at the branching point. [electronic resource] - Carbohydrate research Dec 2016 - 11-19 p. digital
Publication Type: Journal Article
1873-426X
10.1016/j.carres.2016.10.013 doi
Alcohols--chemistry
Carbohydrates--chemistry
Fluorides--chemistry
Fluorine--chemistry
Molecular Structure
Oxidation-Reduction
Stereoisomerism