A caveat on the oxidation of 2,8-diphenyl-1,9,10-anthyridine to 2,8-diphenyl-5(10H)-1,9,10-anthyridone

dc.contributor.author Madhavi, N. N.Laxmi
dc.contributor.author Senthivel, Paramasivam
dc.contributor.author Nangia, Ashwini
dc.date.accessioned 2022-03-27T09:34:07Z
dc.date.available 2022-03-27T09:34:07Z
dc.date.issued 1999-01-01
dc.description.abstract Crystallization of 2,8-diphenyl-1,9,10-anthyridine (1a) from various organic solvents afforded the corresponding anthyridone (2a). The conversion of anthyridine to anthyridone was monitored by 1H NMR spectroscopy in deuterated solvents. It is found that the transformation is facile at ambient temperature and this could be relevant in triply hydrogen-bonded complexes of 1a with neutral and cationic molecules. Copyright © 1999 John Wiley & Sons, Ltd.
dc.identifier.citation Journal of Physical Organic Chemistry. v.12(9)
dc.identifier.issn 08943230
dc.identifier.uri 10.1002/(sici)1099-1395(199909)12:9 < 665::aid-poc172 > 3.0.co;2-u
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/(SICI)1099-1395(199909)12:9 < 665::AID-POC172 > 3.0.CO;2-U
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13062
dc.subject 1 H NMR
dc.subject Anthyridine
dc.subject Anthyridone
dc.subject Oxidation
dc.subject Supramolecular
dc.title A caveat on the oxidation of 2,8-diphenyl-1,9,10-anthyridine to 2,8-diphenyl-5(10H)-1,9,10-anthyridone
dc.type Journal. Article
dspace.entity.type
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