SYNTHESIS OF 1,8-NAPHTHYRIDINES: A RECENT UPDATE

Авторы

  • 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

Ключевые слова:

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

Аннотация

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.

Биография автора

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

Загрузки

Опубликован

2020-09-17

Выпуск

Том 56 № 8 (2020)

Раздел

Гетероциклы в фокусе