ENANTIODIVERGENT SYNTHESIS OF THE KEY INTERMEDIATE FOR A MARINE NATURAL FURANOTERPENE BY CHEMOENZYMATIC PROCESS

Authors
HONDA T OGINO T
Citation
T. Honda et T. Ogino, ENANTIODIVERGENT SYNTHESIS OF THE KEY INTERMEDIATE FOR A MARINE NATURAL FURANOTERPENE BY CHEMOENZYMATIC PROCESS, Tetrahedron : asymmetry, 9(15), 1998, pp. 2663-2669
Citations number
10
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
9
Issue
15
Year of publication
1998
Pages
2663 - 2669
Database
ISI
SICI code
0957-4166(1998)9:15<2663:ESOTKI>2.0.ZU;2-M
Abstract
A short chemoenzymatic route to both enantiomers of the key intermedia te in the preparation of a marine natural furanoterpene was developed by employing a prochiral malonate derivative as a starting material. ( C) 1998 Elsevier Science Ltd. All rights reserved.