Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/4672
Title: BF3·Et2O Ediated One-step Synthesis of N-substituted-1,2-dihydropyridines, Indenopyridines and 5,6-dihydroisoquinolines
Authors: Salfeena, C T F
Ashitha, K T
Sasidhar, B S
Keywords: BF3·Et2O
N-substituted-1,2-dihydropyridines
Issue Date: 2016
Publisher: Royal society of chemistry
Citation: Organic & Biomolecular Chemistry;14(43):10165-10169
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.
URI: https://doi.org/10.1039/c6ob02133f
http://localhost:8080/xmlui/handle/123456789/4672
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