Chemoselectivity in the manipulation of polyhydroxylated compounds derived from the diastereoselective dihydroxylation of optically active allylic enoate alcohols

DOI: 10.1016/0040-4020(96)00357-2

Source and publish data:

Tetrahedron p. 7861 - 7874 (1996)

Update date:2022-08-03

Topics:

Authors:

Barros, M. Teresa

Januario-Charmier, M. Odile

Maycock, Christopher D.

Pires, Mariana

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Article abstract of DOI:10.1016/0040-4020(96)00357-2

An efficient, practical and stereoselective route for the preparation of several polyols and their corresponding lactols and lactones is described. They are promising precursors for the synthesis of several structurally interesting compounds.

Full text of DOI:10.1016/0040-4020(96)00357-2

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