An expeditious enantiospecific synthesis of a precursor of the lactonic portion of mevinic acids

DOI: 10.1016/0040-4039(92)88123-M

Source and publish data:

Tetrahedron Letters p. 1997 - 2000 (1992)

Update date:2022-07-29

Topics:

Authors:

Boquel Boquel

Cazalet, C. Loustau

Chapleur

Samreth Samreth

Bellamy Bellamy

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Article abstract of DOI:10.1016/0040-4039(92)88123-M

A short, enantiospecific synthesis of the methylglycoside 5, a precursor of the lactonic moiety present in all mevinic acids and analogues, starting with 1,6-anhydro-D-glucose is described.

Full text of DOI:10.1016/0040-4039(92)88123-M

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