57042-08-7Relevant articles and documents
Desymmetrizing Hydroformylation of Dihydromuconic Acid Diesters: Application to the Synthesis of (±)-Vindeburnol
Salacz, Laura,Charpentier, Cyrille,Suffert, Jean,Girard, Nicolas
, p. 2257 - 2262 (2017/02/26)
The desymmetrizing hydroformylation of internal alkenes derived from dihydromuconic acid is described. The study of this reaction afforded easy access to polyfunction aldehydes. After the evaluation of the reactivity of the dimethyl ester derivative with various primary amines, this methodology was used to design a rapid synthesis of (±)-vindeburnol from tryptamine in only two steps.
Stereoselective synthesis of (-)-jimenezin
Hwang, Cheol Hee,Keum, Gyochang,Sohn, Kyoung Il,Lee, Dong Hoon,Lee, Eun
, p. 6621 - 6623 (2007/10/03)
Total synthesis of jimenezin was achieved via radical cyclization of β-alkoxyacrylate and β-alkoxyvinyl sulfoxide intermediates and intramolecular olefin metathesis reaction.
Design, synthesis, and conformational analysis of a proposed type I β- turn mimic
Fink, Brian E.,Kym, Phil R.,Katzenellenbogen, John A.
, p. 4334 - 4344 (2007/10/03)
In an effort to design a dipeptide structural mimic of protein and peptide β-turns, we have prepared and evaluated the conformation of derivatives of the novel, highly constrained ten-membered lactam, (3S,10S)- (6E)-2-azacyclodec-6-enone (1). A synthetic