1137089-32-7Relevant academic research and scientific papers
A divergent and stereoselective approach to phenolic 1,7-dihydroxy- bisabolane sesquiterpenes: Asymmetric total synthesis of (+)-curcutetraol, (+)-sydonol, (+)-sydonic acid, and (+)-7-O-methylsydonic acid
Serra, Stefano,Cominetti, Alessandra A.
, p. 1110 - 1116 (2013/10/08)
The combined use of the Sharpless asymmetric epoxidation, a number of stereospecific chemical transformations, and the 3,5-hexadienoic acid benzannulation protocol allowed us to devise a new, divergent, and stereoselective approach to terpenes with a chir
