ENANTIOSELECTIVE SYNTHESIS OF 7-CYCLOOCTEN-1,3,5,6-TETRAOL DERIVATIVES BY ENZYMATIC ASYMMETRIZATION

Authors
JOHNSON CR HARIKRISHNAN LS GOLEBIOWSKI A
Citation
Cr. Johnson et al., ENANTIOSELECTIVE SYNTHESIS OF 7-CYCLOOCTEN-1,3,5,6-TETRAOL DERIVATIVES BY ENZYMATIC ASYMMETRIZATION, Tetrahedron letters, 35(42), 1994, pp. 7735-7738
Citations number
25
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
42
Year of publication
1994
Pages
7735 - 7738
Database
ISI
SICI code
0040-4039(1994)35:42<7735:ESO7D>2.0.ZU;2-4
Abstract
meso-Diol 4, derived from 1,5-cyclooctadiene, in the presence of Pseud omonas cepacia lipase in isopropenyl acetate, afforded enantiopure 5, an attractive intermediate for the synthesis of sugars and related com pounds.