Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2223
Title: SYNTHESIS AND STEREODYNAMICS OF N-FORMYL-1,2,3- SELENADIAZOLOPYRIDINES
Authors: M, Ingarsal
P, Amutha
M, Gopalakrishnan
S, Nagarajan
Keywords: 1,2,3-Selenadiazoles
piperidone
N-formyl compounds
stereodynamics
Issue Date: 31-Jan-2012
Publisher: Taylor & Francis
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
URI: https://doi.org/10.1080/10426507.2011.627899
http://localhost:8080/xmlui/handle/123456789/2223
ISSN: 1563-5325
Appears in Collections:International Journals

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