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.
2015
Catelani, Giorgio; D'Andrea, Felicia; Gragnani, Tiziana; Agnolin, Irene; Guazzelli, Lorenzo
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/750813
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