1422252-99-0Relevant articles and documents
Gold catalyzed stereoselective tandem hydroamination-formal aza-Diels-Alder reaction of propargylic amino esters
Fustero, Santos,Bello, Paula,Miro, Javier,Sanchez-Rosello, Maria,Maestro, Miguel A.,Gonzalez, Javier,Pozo, Carlos Del
, p. 1336 - 1338 (2013/03/13)
A gold-catalyzed tandem intramolecular hydroamination-formal aza-Diels-Alder reaction of propargylic amino esters is described. The overall process leads to the formation of a tetracyclic framework as a single diastereoisomer, with the creation of four bonds and five stereocenters.