1383371-26-3Relevant academic research and scientific papers
An organocatalytic enantioselective synthesis of (+)-duryne
Kumaraswamy, Gullapalli,Sadaiah, Kadivendi,Raghu, Nimmakayala
, p. 587 - 593 (2012/08/13)
An efficient enantioselective synthesis of the potent anticancer agent (+)-duryne was achieved by the use of a one-pot organocatalyzed hydroxylation/Ohira-Bestmann and Grubbs cross-metathesis/selective cis-Wittig reaction. This new approach is envisioned to facilitate the synthesis of every representative member of the family.
