Microbiological transformations. 21. An expedient route to both enantiomers of marmin and epoxyauraptens via microbiological dihydroxylation of 7-geranyloxycoumarin

DOI: 10.1016/S0957-4166(00)80044-0

Source and publish data:

Tetrahedron Asymmetry p. 247 - 250 (1991)

Update date:2022-08-04

Topics:

Authors:

Zhang Zhang

Archelas

Meou Meou

Furstoss

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Article abstract of DOI:10.1016/S0957-4166(00)80044-0

The expedient synthesis of either enantiomers of Marmin or Epoxyauraptens of high enantiomeric purity is described. This was achieved via a stereospecific dihydroxylation of the remote double bond of a geraniol derivative using the fungus Aspergillus niger.

Full text of DOI:10.1016/S0957-4166(00)80044-0

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