SYNTHESIS OF 1,8-NAPHTHYRIDINES: A RECENT UPDATE

Authors

  • Mahesh R. Kulkarni Organic Chemistry Research Centre, Department of Chemistry, K.R.T. Arts, B. H. Commerce and A. M. Science College, Gangapur Road, Nashik 422 002, MS
  • Nitin D. Gaikwad Organic Chemistry Research Centre, Department of Chemistry, K.R.T. Arts, B. H. Commerce and A. M. Science College, Gangapur Road, Nashik 422 002, MS

DOI:

https://doi.org/10.1007/5737

Keywords:

Eaton's reagent, 1, 8-naphthyridine, synthesis

Abstract

This microreview focuses on the recent achievements (2015–2019) toward the synthesis of 1,8-naphthyridines, which include multicomponent reactions, Friedländer approach using green strategy, hydroamination of terminal alkynes followed by Friedländer cyclization, metal-catalyzed synthesis, and ring expansion reaction of 3-substituted 1H-pyrrolo[2,3-b]pyridin-2(3H)-one.

Author Biography

Nitin D. Gaikwad, Organic Chemistry Research Centre, Department of Chemistry, K.R.T. Arts, B. H. Commerce and A. M. Science College, Gangapur Road, Nashik 422 002, MS

Assistant Professor

Department of chemistry

gaikwad.chemistry@gmail.com

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Published

2020-09-17

Issue

Vol. 56 No. 8 (2020)

Section

Heterocycles in Focus