SYNTHESIS AND STEREODYNAMICS OF N-FORMYL-1,2,3- SELENADIAZOLOPYRIDINES

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DC Field	Value	Language
dc.contributor.author	M, Ingarsal	-
dc.contributor.author	P, Amutha	-
dc.contributor.author	M, Gopalakrishnan	-
dc.contributor.author	S, Nagarajan	-
dc.date.accessioned	2020-10-16T08:54:16Z	-
dc.date.available	2020-10-16T08:54:16Z	-
dc.date.issued	2012-01-31	-
dc.identifier.issn	1563-5325	-
dc.identifier.uri	https://doi.org/10.1080/10426507.2011.627899	-
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/2223	-
dc.description.abstract	The 4,6-diaryl-6,7-dihydro-[1,2,3]selenadiazolo[5,4-c]pyridine-5(4H)-carbalde hydes were synthesized from 2,6-diarylpiperidin-4-ones and characterized using infrared, 1H, 13C Nuclear Magnetic Resonance (NMR), and mass spectroscopic techniques. On the NMR time scale, the compounds exist in syn and anti isomeric forms. Separate signals were obtained for isomers in the NMR spectra. The compounds’ stereodynamic nature was studied based on the intensity and position of NMR signals	en_US
dc.language.iso	en	en_US
dc.publisher	Taylor & Francis	en_US
dc.subject	1,2,3-Selenadiazoles	en_US
dc.subject	piperidone	en_US
dc.subject	N-formyl compounds	en_US
dc.subject	stereodynamics	en_US
dc.title	SYNTHESIS AND STEREODYNAMICS OF N-FORMYL-1,2,3- SELENADIAZOLOPYRIDINES	en_US
dc.type	Article	en_US
Appears in Collections:	International Journals

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