BF3·Et2O Ediated One-step Synthesis of N-substituted-1,2-dihydropyridines, Indenopyridines and 5,6-dihydroisoquinolines

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DC Field	Value	Language
dc.contributor.author	Salfeena, C T F	-
dc.contributor.author	Ashitha, K T	-
dc.contributor.author	Sasidhar, B S	-
dc.date.accessioned	2024-01-17T16:41:58Z	-
dc.date.available	2024-01-17T16:41:58Z	-
dc.date.issued	2016	-
dc.identifier.citation	Organic & Biomolecular Chemistry;14(43):10165-10169	en_US
dc.identifier.uri	https://doi.org/10.1039/c6ob02133f	-
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/4672	-
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal society of chemistry	en_US
dc.subject	BF3·Et2O	en_US
dc.subject	N-substituted-1,2-dihydropyridines	en_US
dc.title	BF3·Et2O Ediated One-step Synthesis of N-substituted-1,2-dihydropyridines, Indenopyridines and 5,6-dihydroisoquinolines	en_US
dc.type	Article	en_US
Appears in Collections:	2016

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