SYNTHESIS OF THE ENANTIOMERS OF UMBELACTONE. CONFIGURATIONAL ASSIGNMENT OF THE NATURAL PRODUCT.

DOI: 10.1016/S0040-4020(01)86802-2

Source and publish data:

Tetrahedron p. 2199 - 2202 (1987)

Update date:2022-09-26

Topics:

Authors:

Ortuno, Rosa M.

Bigorra, Joaquim

Font, Josep

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Article abstract of DOI:10.1016/S0040-4020(01)86802-2

Both (+)- and (-)-umbelactone have been synthetized from (R)-γ-hydroxymethyl-γ-butyrolactone and D-ribonolactone, respectively.The absolute configuration of the natural product has shown to be R-(+).

Full text of DOI:10.1016/S0040-4020(01)86802-2

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