%0 Journal Article
%T Novel Tandem Three Consecutive Reactions: Aza-Wittig, Imine Condensation and Electrophilic Aromatic Substitution Strategy to Indolizine Synthesis
%A Julio C. Gonz¨¢lez-Rodr¨ªguez
%A Carlos Gonz¨¢lez-Romero
%A Erick Cuevas-Y¨¢£¿ez
%A Juan J. Mej¨ªa Vega
%A Christopher K. Jankowski
%A David Corona-Becerril
%J International Journal of Organic Chemistry
%P 55-71
%@ 2161-4695
%D 2021
%I Scientific Research Publishing
%R 10.4236/ijoc.2021.112006
%X Reaction</span><span style=\"font-family:&quot;\"><span style=\"font-family:Verdana;\"> of ethyl
(Z)-3-(heteroaryl/aryl)-2-((triphenyl-</span><i><span style=\"font-family:Verdana;\">¦Ë</span></i><sup><span style=\"font-family:Verdana;\">5</span></sup><span style=\"font-family:Verdana;\">-phosphaneylidene) amino) acrylates
intermediates with 2,3-thiophenedicarboxaldehyde
w</span></span><span style=\"font-family:Verdana;\">as</span><span style=\"font-family:Verdana;\"> used</span><span style=\"font-family:Verdana;\"> in novel Tandem three
consecutive reactions: aza-Wittig, imine condensation and electrophilic heteroaromatic cyclization to obtain a series of
indolizines. A tentative mechanism of this reaction is proposed.
%K Iminophosphorane
%K Tandem Reaction
%K Indolizine Synthesis
%U http://www.scirp.org/journal/PaperInformation.aspx?PaperID=110262