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He, L., Yang, Y., Liu, X., Liang, G., Li, C., Wang, D. and Pan, W. (2015) Iodine-Mediated Oxidative Cyclization of 2-(Pyridin-2-yl)acetate Derivatives with Alkynes: Condition-Controlled Selective Synthesis of Multisubstituted Indolizines. Synthesis, 52, 459-470.
https://doi.org/10.1055/s-0039-1690229
has been cited by the following article:
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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.