Microbial Transformations 16. One-step synthesis of a pivotal prostaglandin chiral synthon via a highly enantioselective microbiological Baeyer-Villiger type reaction

DOI: 10.1016/S0040-4039(01)80476-7

Source and publish data:

Tetrahedron Letters p. 3663 - 3664 (1989)

Update date:2022-08-11

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Authors:

Alphand, Veronique

Archelas, Alain

Furstoss, Roland

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Article abstract of DOI:10.1016/S0040-4039(01)80476-7

The bioconversion of bicyclo<3.2.0>hept-2-en-6-one is described.Each one of its enantiomers affords a different lactone via a highly regio and enantiospecific Beayer-Villiger type process.

Full text of DOI:10.1016/S0040-4039(01)80476-7

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