Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.crci.2010.10.003
DC FieldValue
dc.titleSynthesis and tautomerism study of 6-benzoylmethyl-1,3,5-triazin-2,4- diamine
dc.contributor.authorSachdeva, N.
dc.contributor.authorDolzhenko, A.V.
dc.contributor.authorChui, W.K.
dc.date.accessioned2014-10-29T01:59:19Z
dc.date.available2014-10-29T01:59:19Z
dc.date.issued2011-06
dc.identifier.citationSachdeva, N., Dolzhenko, A.V., Chui, W.K. (2011-06). Synthesis and tautomerism study of 6-benzoylmethyl-1,3,5-triazin-2,4- diamine. Comptes Rendus Chimie 14 (6) : 580-587. ScholarBank@NUS Repository. https://doi.org/10.1016/j.crci.2010.10.003
dc.identifier.issn16310748
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/106400
dc.description.abstractFrom the reaction of biguanide with ethyl benzoylacetate, N-(6-oxo-4-phenyl-1,6-dihydropyrimidin-2-yl)guanidine (1) and 6-benzoylmethyl-1,3,5-triazin-2,4-diamine (2) were isolated. The structural evaluation of 2 was performed theoretically (DFT calculations) and experimentally (NMR spectroscopy and X-ray crystallography). The effects of solvents and temperature on keto-enol-enaminone tautomeric equilibrium were explored. © 2010 Académie des sciences. Published by Elsevier Masson SAS. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.crci.2010.10.003
dc.sourceScopus
dc.subjectDFT calculations
dc.subjectResonance-assisted hydrogen bonding
dc.subjectSolvent effect
dc.subjectTautomerism
dc.subjectTriazines
dc.subjectX-ray crystal structure
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.doi10.1016/j.crci.2010.10.003
dc.description.sourcetitleComptes Rendus Chimie
dc.description.volume14
dc.description.issue6
dc.description.page580-587
dc.description.codenCRCOC
dc.identifier.isiut000293153000009
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