RESOLUTION OF RACEMIC 2,6,6-TRIMETHYL-7-OXA-BICYCLO[3.1.1]OCTAN-2-OL AND 1,6,6-TRIMETHYL-7-OXA-BICYCLO[3.1.1]OCTAN-2-OL BY MICROBIAL ESTERIFICATION

Authors
MIYAZAWA M TSURUNO K KAMEOKA H
Citation
M. Miyazawa et al., RESOLUTION OF RACEMIC 2,6,6-TRIMETHYL-7-OXA-BICYCLO[3.1.1]OCTAN-2-OL AND 1,6,6-TRIMETHYL-7-OXA-BICYCLO[3.1.1]OCTAN-2-OL BY MICROBIAL ESTERIFICATION, Tetrahedron : asymmetry, 8(13), 1997, pp. 2131-2132
Citations number
2
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
8
Issue
13
Year of publication
1997
Pages
2131 - 2132
Database
ISI
SICI code
0957-4166(1997)8:13<2131:ROR2A>2.0.ZU;2-O
Abstract
Resolution of racemic 2,6,6-trimethyl-7-oxa-bicyclo[3.1.1]octan-2-ol a nd racemic 1,6,6-trimethyl-7-oxa-bicyclo[3.1.1]octan-2-ol via esterifi cation with malonic acid by Glomerella cingulata, is described. Both o f alcohols and malonic esters could be obtained in enantiomerically pu re states. (C) 1997 Elsevier Science Ltd.