1204591-95-6Relevant academic research and scientific papers
Preparation, modification, and evaluation of cruentaren a and analogues
Bindl, Martin,Jean, Ludovic,Herrmann, Jennifer,Mueller, Rolf,Fuerstner, Alois
supporting information; experimental part, p. 12310 - 12319 (2010/05/02)
An expeditious total synthesis of the highly cytotoxic F-ATPase inhibitor cruentaren A. (1) is described based on a. ring-closing alkyne metathesis (RCAM) reaction for the formation of the macrocylic ring. Other key transformations comprise a. C-acylation
