STEREOSELECTIVE SYNTHESIS OF Y-3-(3,4-METHYLENEDIOXYBENZYL)-GAMMA-BUTYROLACTONE FROM L-(-ARABINOSE VIA A CARISSANOL-TYPE OF LIGNAN())

Authors
YAMAUCHI S KINOSHITA Y
Citation
S. Yamauchi et Y. Kinoshita, STEREOSELECTIVE SYNTHESIS OF Y-3-(3,4-METHYLENEDIOXYBENZYL)-GAMMA-BUTYROLACTONE FROM L-(-ARABINOSE VIA A CARISSANOL-TYPE OF LIGNAN()), Bioscience, biotechnology, and biochemistry, 62(3), 1998, pp. 521-525
Citations number
14
Categorie Soggetti
Biology,Agriculture,"Biothechnology & Applied Migrobiology","Food Science & Tenology
Journal title
Bioscience, biotechnology, and biochemistry → ACNP
ISSN journal
09168451
Volume
62
Issue
3
Year of publication
1998
Pages
521 - 525
Database
ISI
SICI code
0916-8451(1998)62:3<521:SSOY>2.0.ZU;2-B
Abstract
As a model experiment for the synthesis of optically active ha,beta-di benzyl-alpha-hydroxy-gamma-butyrolactone (1), (2S,3S)-2-benzyl-2-hydro xy-3-(3 ,4-methylenedioxybenzyl)-gamma-butyrolactone (3) was stereosel ectively synthesized from L-(+)-arabinose via the carissanol-type of l ignan, ydroxy-4-(3,4-methylenedioxybenzyl)tetrahydrofuran (4).