767330-06-3Relevant academic research and scientific papers
Lipase-catalyzed resolution of 1-[4-(benzyloxy)phenyl]hex-5-en-3-ol: Synthesis of (-)-centrolobine
Tadiparthi, Krishnaji,Raghavendra,Kamal, Ahmed
, p. 2321 - 2326 (2017/10/06)
A practical and efficient method for the preparation of homoallylic alcohol and its successful enzymatic resolution has been developed. This lipase-catalyzed resolution process has been optimized with respect to different lipases and solvents. Moreover, M
Total synthesis of (-)-centrolobine: β-C-glycoside formation via a tandem Grignard addition and stereoselective hemi-ketal reduction
Jennings, Michael P.,Clemens, Ryan T.
, p. 2021 - 2024 (2007/10/03)
It has been demonstrated that an aryl-β-C-glycoside can be efficiently constructed via a sequence consisting of Brown asymmetric allylation, ring-closing metathesis, hydrogenation, nucleophilic addition, and stereoselective Et3SiH reduction. Th
Two successive one-pot reactions leading to the expeditious synthesis of (-)-centrolobine
Boulard, Lucie,Bouzbouz, Samir,Cossy, Janine,Franck, Xavier,Figadère, Bruno
, p. 6603 - 6605 (2007/10/03)
A very short and efficient synthesis of (-)-centrolobine has been achieved by using two successive one-pot reactions. The first sequence involves a cross-metathesis reaction/hydrogenation/lactonization and the second sequence is a Grignard addition/reduct
