96917-15-6Relevant articles and documents
Total synthesis of (±)-agastinol
Ding, Junwei,Zhou, Haitang,Jiao, Bin,Xia, Yamu
, p. 352 - 354 (2011)
A synthesis of the tetrahydrofuran lignan (±)-agastinol, starting from the cheap Vanillin, has been developed based on Stobbe reaction with diethyl succinate to give the skeleton of lignan, which was then reduced to afford meso- and threo-(±)-secoisolanciresinol. threo-(±)- Secoisolanciresinol was treated with DDQ in acetic acid to give the 2-aryl tetrahydrofuran lignan, and which was then condensed with ferulic acid to give (±)-agastinol for the first time.
Synthesis of threo-(±)-9,9-dibenzoylsecoisolariciresinol and its isomer
Xia, Yamu,Wen, Yanling
experimental part, p. 606 - 609 (2011/02/28)
The total synthesis of threo-(±)-9,9-dibenzoylsecoisolariciresinol and its isomer based on two Stobbe reactions as C-C bond-forming steps used a protected vanillin and diethyl; succinate to give the skeleton of lignan, followed by reduction to afford threo-and meso-(±)-secoisolariciresinol Both were treated with benzoyl chloride to obtain the natural product threo-(±)-9,9-dibenzoylsecoisolariciresinol and Its isomer meso-(±)-9,9-dibenzoylsecoisolariciresinol for the first time.
LIGNAN FROM CALYCES OF DIOSPYROS KAKI
Matsuura, Shin,Iinuma, Munekazu
, p. 626 - 628 (2007/10/02)
Key Word Index - Diospyros kaki; Ebenaceae; calyx; (-)-divanillyltetrahydrofuran ferulate. - From Diospyros kaki calyces, a new lignan was isolated.Its structure was elucidated as (-)-divanyllyltetrahydrofuran ferulate by spectroscopic methods and was established by total synthesis.