New synthesis on the basis 2-allyloxy chalcone and NMR studies its some derivatives

Copyright © 2014 John Wiley & Sons, Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 53(2015), 2 vom: 04. Feb., Seite 147-53
1. Verfasser: Mamedov, I G (VerfasserIn)
Weitere Verfasser: Bayramov, M R, Mamedova, Y V, Maharramov, A M
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2015
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article NMR spectroscopy chalcone conformational transition cyclohexenone flavanone hydrogen bond indazole isoxazol keto-enol tautomerism molecular dynamics
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520 |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 
650 4 |a Journal Article 
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650 4 |a conformational transition 
650 4 |a cyclohexenone 
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650 4 |a indazole 
650 4 |a isoxazol 
650 4 |a keto-enol tautomerism 
650 4 |a molecular dynamics 
700 1 |a Bayramov, M R  |e verfasserin  |4 aut 
700 1 |a Mamedova, Y V  |e verfasserin  |4 aut 
700 1 |a Maharramov, A M  |e verfasserin  |4 aut 
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