A short synthesis of substituted β-hydroxy γ-butyrolactones and 2-deoxyhexofuranosides

DOI: 10.1016/S0040-4039(00)91641-1

Source and publish data:

Tetrahedron Letters p. 1439 - 1442 (1992)

Update date:2022-08-04

Topics:

Authors:

Escudier

Baltas Baltas

Gorrichon

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Article abstract of DOI:10.1016/S0040-4039(00)91641-1

The γ,δ-epoxy β-hydroxyesters obtained by diastereselective aldolisation between ester enolates and optically active α,β-epoxyaldehydes, undergo quantitative stereocontrolled lactonisation which can be followed by reduction to provide 2-deoxy hexofuranosi

Full text of DOI:10.1016/S0040-4039(00)91641-1

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