ENANTIOSELECTIVE SYNTHESIS OF THE HYDROXYL-LACTONE MOIETY OF MEVINIC ACIDS

Authors
MCCAGUE R OLIVO HF ROBERTS SM
Citation
R. Mccague et al., ENANTIOSELECTIVE SYNTHESIS OF THE HYDROXYL-LACTONE MOIETY OF MEVINIC ACIDS, Tetrahedron letters, 34(23), 1993, pp. 3785-3786
Citations number
19
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
23
Year of publication
1993
Pages
3785 - 3786
Database
ISI
SICI code
0040-4039(1993)34:23<3785:ESOTHM>2.0.ZU;2-T
Abstract
2-Oxa-4endo-hydroxybicyclo[3.3.0]-oct-7-en-3-one was resolved with Pse udomonas fluorescens lipase and one of the enantiomers was converted i nto a key intermediate in the synthesis of mevinic acids.