74683-15-1Relevant academic research and scientific papers
An asymmetric route to total synthesis of the furano lignan (+)-veraguensin
Matcha, Kiran,Ghosh, Subrata
, p. 6924 - 6927 (2011/03/18)
Total synthesis of the furano lignan (+)-veraguensin is described. The key steps involve a diastereoselective aldol-type condensation of an ester enolate having an α-chiral center with an aromatic aldehyde and a novel isomerization of the syn vicinal subs
An acyl-claisen approach to tetrasubstituted tetrahydrofuran lignans: Synthesis of fragransin A2, talaumidin, and lignan analogues
Rye, Claire E.,Barker, David
scheme or table, p. 3315 - 3319 (2010/03/04)
A simple and stereocontrolled synthesis of racemic 2,3,4,5-tetrasubstituted tetrahydrofurans was achieved from acyl-Claisen derived syn-disubstituted amides. Georg Thieme Verlag Stuttgart New York.
Stereoselective synthesis of tetrahydrofuran lignans via BF 3·OEt2-promoted reductive deoxygenation/ epimerization of cyclic hemiketal: Synthesis of (-)-odoratisol C, (-)-futokadsurin A, (-)-veraguensin, (+)-fragransin A2, (+)-galbel
Kim, Hyoungsu,Wooten, Ceshea M.,Park, Yongho,Hong, Jiyong
, p. 3965 - 3968 (2008/02/11)
A versatile route to the synthesis of 2,5-diaryl-3,4- dimethyltetrahydrofuran lignans, (-)-odoratisol C. (1), (-)-futokadsurin A (2), (-)-veraguensln (3), (+)-fragransin A2 (4), (+)-galbelgin (5), and (+)-talaumidin (6), is described. Central t
