954114-85-3Relevant articles and documents
Synthesis of γ-Lactones via the kowalski homologation reaction: Protecting-group-free divergent total syntheses of eupomatilones-2,5,6, and 3- epi-eupomatilone-6
Choi, Hosam,Jang, Hanho,Kim, Hyoungsu,Lee, Kiyoun
supporting information, p. 7857 - 7862 (2019/10/11)
A highly efficient synthesis of functionalized chiral γ-butyrolactone scaffolds has been described. The basis of the approach is the Kowalski ester homologation that is modified for our proposed transformation. The newly developed methodology combines a d
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