ISOLATION, STRUCTURE ELUCIDATION, AND CHEMICAL DERIVATIZATION OF A NEW CYCLIC BISBIBENZYL DIMER, PUSILATIN-E, FROM THE LIVERWORT RICCARDIA-MULTIFIDA SUBSP DECRESCENS

Citation
T. Yoshida et al., ISOLATION, STRUCTURE ELUCIDATION, AND CHEMICAL DERIVATIZATION OF A NEW CYCLIC BISBIBENZYL DIMER, PUSILATIN-E, FROM THE LIVERWORT RICCARDIA-MULTIFIDA SUBSP DECRESCENS, Journal of natural products, 60(2), 1997, pp. 145-147
Citations number
12
Categorie Soggetti
Chemistry,"Plant Sciences","Pharmacology & Pharmacy","Chemistry Medicinal
Journal title
ISSN journal
01633864
Volume
60
Issue
2
Year of publication
1997
Pages
145 - 147
Database
ISI
SICI code
0163-3864(1997)60:2<145:ISEACD>2.0.ZU;2-B
Abstract
A new cyclic bisbibenzyl dimer (1) has been isolated from the MeOH ext ract of the liverwort Riccardia multifida subsp. decrescens, together with two previously known bisbibenzyls [riccardin A (2) and marchantin I (3)] and a norneolignan [egonol 2-methylbutanoate (4)]. Extensive H -1- and C-13-NMR spectral measurements and chemical derivatization all owed the structure of dimeric riccardin A to be defined; it has been n amed pusilatin E (1).