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