Tetrahedron Letters

An efficient catalytic method for the Friedländer annulation mediated by peptide coupling agent propylphosphonic anhydride (T3P®)

JK Augustine, A Bombrun, S Venkatachaliah

Index: Augustine, John Kallikat; Bombrun, Agnes; Venkatachaliah, Srinivasa Tetrahedron Letters, 2011 , vol. 52, # 50 p. 6814 - 6818

Full Text: HTML

Citation Number: 21

Abstract

We have demonstrated the utilization of T3P, a mild and low toxic peptide coupling agent, as a promoter and water scavenger in the Friedländer annulation, and thus introduced a highly efficient catalytic process to access carbocyclic and heterocyclic fused quinolines under microwave irradiation or a conventional heating technique. The reaction conditions are sufficiently mild to tolerate the acid and base sensitive functional groups that can serve as ...

Related Articles:

4+ 1 Radical annulations with isonitriles: a simple route to cyclopenta-fused quinolines

[Curran, Dennis P.; Liu, Hui Journal of the American Chemical Society, 1991 , vol. 113, # 6 p. 2127 - 2132]

A mild, efficient and improved protocol for the friedländer synthesis of quinolines using lewis acidic ionic liquid

[Karthikeyan, Ganesan; Perumal, Paramasivan T. Journal of Heterocyclic Chemistry, 2004 , vol. 41, # 6 p. 1039 - 1041]

More Articles...