109547-79-7Relevant articles and documents
Formal [4+2]-annulation of vinyl azides with N-unsaturated aldimines
Zhu, Xu,Wang, Yi-Feng,Zhang, Feng-Lian,Chiba, Shunsuke
supporting information, p. 2458 - 2462 (2014/10/15)
Highly functionalized quinolines and pyridines could be synthesized by BF3?OEt2-mediated reactions of vinyl azides with N-aryl and N-alkenyl aldimines, respectively. The reaction mechanism could be characterized as formal [4+2]-annulation, including unprecedented enamine-type nucleophilic attack of vinyl azides to aldimines and subsequent nucleophilic cyclization onto the resulting iminodiazonium ion moieties.
An Efficient Iminophosphorane-Mediated Synthesis of Thienopyridine, Thienopyridine and Furopyridine Derivatives
Molina, P.,Fresneda, P. M.,Hurtado, F.
, p. 45 - 48 (2007/10/02)
A number of thienopyridines 4, thienopyridines 7 and furopyridines 11 derivatives have been prepared by reaction of the appropriate iminophosphorane, available from ethyl azidoheteroarylacrylates and triphenylphosphine, with aromatic