2021
DOI: 10.1016/j.ica.2020.120207
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Synthesis and characterization of copper (II) complexes with arylmethylenebis-4-hydroxy-6-methyl-2-N-pyran-2-ones: A case of interesting keto-enol tautomerism

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Cited by 4 publications
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“…5 ). As an electron-withdrawing group, although the carbonyl group (C=O) would make the hydrogen on its adjacent atoms exhibit considerable activity and dissociate more easily ( 55 , 56 , 57 ), the carbonyl (C=O) group has been used to prepare biologically active ABA-photoaffinity labels ( 58 , 59 ). In summary, the process of the ABA–protein interaction in the binding pocket is mainly dependent on the carboxyl (-COOH) and hydroxyl (-OH) groups of ABA, rather than its carbonyl group (C=O).…”
Section: Discussionmentioning
confidence: 99%
“…5 ). As an electron-withdrawing group, although the carbonyl group (C=O) would make the hydrogen on its adjacent atoms exhibit considerable activity and dissociate more easily ( 55 , 56 , 57 ), the carbonyl (C=O) group has been used to prepare biologically active ABA-photoaffinity labels ( 58 , 59 ). In summary, the process of the ABA–protein interaction in the binding pocket is mainly dependent on the carboxyl (-COOH) and hydroxyl (-OH) groups of ABA, rather than its carbonyl group (C=O).…”
Section: Discussionmentioning
confidence: 99%