USE OF ALDOLASES IN THE SYNTHESIS OF NONCARBOHYDRATE NATURAL-PRODUCTS- STEREOSELECTIVE SYNTHESIS OF ASPICILIN C-3-C-9 FRAGMENT

Authors
CHENEVERT R LAVOIE M DASSER M
Citation
R. Chenevert et al., USE OF ALDOLASES IN THE SYNTHESIS OF NONCARBOHYDRATE NATURAL-PRODUCTS- STEREOSELECTIVE SYNTHESIS OF ASPICILIN C-3-C-9 FRAGMENT, Canadian journal of chemistry, 75(1), 1997, pp. 68-73
Citations number
23
Categorie Soggetti
Chemistry
Journal title
Canadian journal of chemistry → ACNP
ISSN journal
00084042
Volume
75
Issue
1
Year of publication
1997
Pages
68 - 73
Database
ISI
SICI code
0008-4042(1997)75:1<68:UOAITS>2.0.ZU;2-Z
Abstract
The C-3 - C-9 main fragment of aspicilin was prepared via a fructose 1 ,6-diphosphate aldolase reaction. The same fragment was also synthesiz ed by chemical transformation starting from D-arabinose.