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231224s2015 xx |||||o 00| ||eng c |
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|a 10.1002/mrc.4172
|2 doi
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|a pubmed24n0811.xml
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|a (DE-627)NLM243300662
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|a (NLM)25371391
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Mamedov, I G
|e verfasserin
|4 aut
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|a New synthesis on the basis 2-allyloxy chalcone and NMR studies its some derivatives
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|c 2015
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 21.05.2015
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|a Date Revised 23.01.2015
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a Copyright © 2014 John Wiley & Sons, Ltd.
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|a Synthesis and NMR investigations of cyclohexenone, flavanone, isoxazol and indazole derivatives of (2E)-3-[2-(allyloxy)-5-bromophenyl]-1-(2-hydroxy-5-methylphenyl)-2-propen-1-one (I, chalcone) have been carried out. The results confirm the formation of O-H•••O type intramolecular hydrogen bond and intramolecular cyclization in the (2E)-3-[2-(allyloxy)-5-bromophenyl]-1-(2-hydroxy-5-methylphenyl)-2-propen-1-one (I), the presence of conformational and keto-enol tautomeric transitions in the 6-acetyl-5-[2-(allyloxy)-5-bromophenyl]-3-(2-hydroxy-5-methylphenyl)-2-cyclohexen-1-one (II), conformational transitions in the 2-{4-[2-(allyloxy)-5-bromophenyl]-3-methyl-4.5-dihydro-1.2-benzisoxazol-6-yl}-4-methylphenol (III) and 2-{4-[2-(allyloxy)-5-bromophenyl]-3-methyl-4.5-dihydro-1H-indazol-6-yl}-4-methylphenol (IV). The conformational and keto-enol tautomerism in the investigated compounds have been also confirmed by chemical methods
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|a Journal Article
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|a NMR spectroscopy
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|a chalcone
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|a conformational transition
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|a cyclohexenone
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|a flavanone
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|a hydrogen bond
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|a indazole
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|a isoxazol
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|a keto-enol tautomerism
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|a molecular dynamics
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|a Bayramov, M R
|e verfasserin
|4 aut
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|a Mamedova, Y V
|e verfasserin
|4 aut
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|a Maharramov, A M
|e verfasserin
|4 aut
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|i Enthalten in
|t Magnetic resonance in chemistry : MRC
|d 1985
|g 53(2015), 2 vom: 04. Feb., Seite 147-53
|w (DE-627)NLM098179667
|x 1097-458X
|7 nnns
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|g volume:53
|g year:2015
|g number:2
|g day:04
|g month:02
|g pages:147-53
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|u http://dx.doi.org/10.1002/mrc.4172
|3 Volltext
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