Please use this identifier to cite or link to this item: 10.3390/molecules16098041
Title: Intramolecular C-H⋯O hydrogen bonding in 1,4-dihydropyridine derivatives
Authors: Petrova, Marina
Muhamadejev, Ruslan
Vigante, Brigita
Cekavicus, Brigita
Plotniece, Aiva
Duburs, Gunars
Liepinsh, Edvards
Keywords: 1,4-dihydropyridines;Bromination;Hydrogen bond;NMR spectra;Nucleophilic substitution;Quantum chemical calculations;1.4 Chemical sciences;1.6 Biological sciences;3.1 Basic medicine;1.1. Scientific article indexed in Web of Science and/or Scopus database;Analytical Chemistry;Chemistry (miscellaneous);Molecular Medicine;Pharmaceutical Science;Drug Discovery;Physical and Theoretical Chemistry;Organic Chemistry
Issue Date: Sep-2011
Citation: Petrova , M , Muhamadejev , R , Vigante , B , Cekavicus , B , Plotniece , A , Duburs , G & Liepinsh , E 2011 , ' Intramolecular C-H⋯O hydrogen bonding in 1,4-dihydropyridine derivatives ' , Molecules , vol. 16 , no. 9 , pp. 8041-8052 . https://doi.org/10.3390/molecules16098041
Abstract: The diastereotopy of the methylene protons at positions 2 and 6 in 1,4-dihydropiridine derivatives with various substituents has been investigated. NMR spectroscopy and quantum chemistry calculations show that the CH⋯O intramolecular hydrogen bond is one of the factors amplifying the chemical shift differences in the 1H-NMR spectra.
DOI: 10.3390/molecules16098041
ISSN: 1420-3049
Appears in Collections:Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure

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