The regioselective acetone elimination reaction represents an efficient way to prepare 4-deoxy-hex-4-enopyranoside enol ethers with either the threo and the erythro configuration starting from fully protected 3,4-O-isopropylidene-galacto- or talopyranosides respectively.
Regioselective Preparation of 4-Deoxy-erythro-hex-4-enopyranoside Enol Ethers through Acetone Elimination
CATELANI, GIORGIO;D'ANDREA, FELICIA;GUAZZELLI, LORENZO
2015-01-01
Abstract
The regioselective acetone elimination reaction represents an efficient way to prepare 4-deoxy-hex-4-enopyranoside enol ethers with either the threo and the erythro configuration starting from fully protected 3,4-O-isopropylidene-galacto- or talopyranosides respectively.File in questo prodotto:
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