First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol

Authors
Yamauchi, S Kinoshita, Y
Citation
S. Yamauchi et Y. Kinoshita, First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol, BIOS BIOT B, 65(7), 2001, pp. 1559-1567
Citations number
5
Categorie Soggetti
Agricultural Chemistry","Biochemistry & Biophysics
Journal title
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
ISSN journal
09168451 → ACNP
Volume
65
Issue
7
Year of publication
2001
Pages
1559 - 1567
Database
ISI
SICI code
0916-8451(200107)65:7<1559:FSSO(C>2.0.ZU;2-S
Abstract
(+)-Magnostellin C, which is a tetrahydrofuran type of lignan bearing a chi ral secondary benzylic hydroxy group, was stereoselectively synthesized fro m L-arabinose by using threo selective aldol condensation.