A new series of thio-substituted sugars were synthesised relying on the totally regio- and stereoselective cycloaddition of 4-deoxyhex-4-enopyranose derivatives to ‘in situ’ generated oxothiones. Conformational studies of the above unsaturated sugars showed a marked prevalence of the all-axial conformer.

Conformational evaluation of some 4-deoxy-hex-4-enopyranosides derivatives and their use in the preparation of a previously undescribed class of 3-thio-L-sorbopyranosides and 6-C-methoxy analogues

CATELANI, GIORGIO;D'ANDREA, FELICIA;
2003

Abstract

A new series of thio-substituted sugars were synthesised relying on the totally regio- and stereoselective cycloaddition of 4-deoxyhex-4-enopyranose derivatives to ‘in situ’ generated oxothiones. Conformational studies of the above unsaturated sugars showed a marked prevalence of the all-axial conformer.
Capozzi, G; Catelani, Giorgio; D'Andrea, Felicia; Menichetti, S; Nativi, C.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/205929
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