1052707-92-2Relevant academic research and scientific papers
Synthetic studies on Et-743. Assembly of the pentacyclic core and a formal total synthesis
Fishlock, Dan,Williams, Robert M.
supporting information; experimental part, p. 9594 - 9600 (2009/04/07)
(Chemical Equation Presented) A formal total synthesis of the potent anticancer agent Et-743 is described. The tetrahydroisoquinoline core is stereoselectively constructed using a novel radical cyclization of a glyoxalimine. Further elaboration of this core rapidly accessed the pentacyclic core of Et-743, but a mixture of regiosisomers was obtained in the key Pictet-Spengler ring closure. A known advanced intermediate in the synthesis of Et-743 was intercepted, constituting a formal synthesis of the molecule.
