1260694-74-3Relevant academic research and scientific papers
Enantioselective synthesis of the lomaiviticin aglycon full carbon skeleton reveals remarkable remote substituent effects during the dimerization event
Lee, Hong Geun,Ahn, Jae Young,Lee, Amy S.,Shair, Matthew D.
, p. 13058 - 13062 (2010)
A full carbon skeleton of the natural product lomaiviticin has been synthesized. The approach features anionic annulation reactions to deliver A and B rings of the natural product, and stereoselective oxidative enolate coupling to form the central C2-C2′
