1394166-94-9Relevant academic research and scientific papers
Synthesis and Molecular Editing of Callyspongiolide, Part 1: The Alkyne Metathesis/trans-Reduction Strategy
Mata, Guillaume,W?lfl, Bernhard,Fürstner, Alois
, p. 246 - 254 (2019/01/04)
A path-scouting investigation into the highly cytotoxic marine macrolide callyspongiolide is reported that capitalizes on the selective formation of the C10?C11 alkene site. While the closure of the macrocycle by ring closing alkyne metathesis (RCAM) with
The first stereoselective total synthesis of the immunosuppressive decalin derivative monascusic acid B 1
Kumar, Jayprakash Narayan,Das, Biswanath
supporting information, p. 863 - 865 (2014/04/17)
The first stereoselective total synthesis of the immunosuppressive decalin derivative monascusic acid B has been accomplished from (R)-(+)-pulegone involving Horner-Wadsworth-Emmons and Julia-Kocienski olefination reactions and Lewis acid catalyzed intramolecular Diels-Alder cyclization. Georg Thieme Verlag Stuttgart New York.
