Issue 43, 2016

BF3·Et2O mediated one-step synthesis of N-substituted-1,2-dihydropyridines, indenopyridines and 5,6-dihydroisoquinolines

Abstract

A simple and efficient one-pot synthesis of N-substituted-1,2-dihydropyridines, indenopyridines and 5,6-dihydroisoquinolines by a BF3·Et2O mediated novel methodology, from easily available α,β-unsaturated ketones/arylidene ketones, phenyl acetylenes and substituted nitriles, has been described. This novel annulation provides quick access to complex polycyclic frameworks with an excellent substrate scope.

Graphical abstract: BF3·Et2O mediated one-step synthesis of N-substituted-1,2-dihydropyridines, indenopyridines and 5,6-dihydroisoquinolines

Supplementary files

Article information

Article type
Communication
Submitted
30 Sep 2016
Accepted
06 Oct 2016
First published
06 Oct 2016

Org. Biomol. Chem., 2016,14, 10165-10169

BF3·Et2O mediated one-step synthesis of N-substituted-1,2-dihydropyridines, indenopyridines and 5,6-dihydroisoquinolines

C. T. Fathimath Salfeena, K. T. Ashitha and B. S. Sasidhar, Org. Biomol. Chem., 2016, 14, 10165 DOI: 10.1039/C6OB02133F

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