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Jadhay, A.H., Atar, A.B. and Kang, J. (2015) A [bmim]Cl-Promoted Domino Protocol Using an Isocyanide-Based [4+1]-cycloaddition Reaction for the Synthesis of Diversely Functionalized 3-alkylamino-2-alkyl/aryl/hetero-aryl Indolizine-1-carbonitriles under Solvent-Free Conditions. New Journal of Chemistry, 44, 3241-3248.
https://doi.org/10.1039/C9NJ05738B

has been cited by the following article:

• TITLE: Novel Tandem Three Consecutive Reactions: Aza-Wittig, Imine Condensation and Electrophilic Aromatic Substitution Strategy to Indolizine Synthesis

  AUTHORS: Julio C. González-Rodríguez, Carlos González-Romero, Erick Cuevas-Yáñez, Juan J. Mejía Vega, Christopher K. Jankowski, David Corona-Becerril

  KEYWORDS: Iminophosphorane, Tandem Reaction, Indolizine Synthesis

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.11 No.2, June 30, 2021

  ABSTRACT: Reaction of ethyl (Z)-3-(heteroaryl/aryl)-2-((triphenyl-λ5-phosphaneylidene) amino) acrylates intermediates with 2,3-thiophenedicarboxaldehyde was used 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.