NMR spectral study of the structure of 2-amino-4-thiazolinones
AbstractAbstract
[en] As a consequence of partial double bond nature of the exocyclic C-N bond, 2-methyl-amino-4-thiazolinone exists in DMSO-D6 as a mixture of E and Z conformers of the amino form with predominance of the sterically favored E conformer. 2-Phenylimino-4-thiazolidinone in the same solvent exists as a mixture of the E and Z isomers of the imino form
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Translated from Khim. Geterotsikl. Soedin.; 22: No.4, 544-548(Apr 1986).
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Journal Article
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Descriptors (DEI)
AMINES, CARBON 13, CHEMICAL SHIFT, CHLOROFORM, COUPLING CONSTANTS, DEUTERIUM COMPOUNDS, DMSO, ELECTRONIC STRUCTURE, HEAVY WATER, HYDROGEN 1, HYDROGEN TRANSFER, HYPERFINE STRUCTURE, IMINES, ISOMERS, ISOTOPIC EXCHANGE, J-J COUPLING, KETONES, MOLECULAR STRUCTURE, MULTIPLETS, NMR SPECTRA, ORGANIC SOLVENTS, PROTONS, SOLVATION, TEMPERATURE DEPENDENCE, THIAZOLES
Descriptors (DEC)
AZOLES, BARYONS, CARBON ISOTOPES, CATIONS, CHARGED PARTICLES, COUPLING, ELEMENTARY PARTICLES, EVEN-ODD NUCLEI, FERMIONS, HADRONS, HETEROCYCLIC COMPOUNDS, HYDROGEN COMPOUNDS, HYDROGEN IONS, HYDROGEN IONS 1 PLUS, HYDROGEN ISOTOPES, INTERMEDIATE COUPLING, IONS, ISOTOPES, LIGHT NUCLEI, NONAQUEOUS SOLVENTS, NUCLEI, NUCLEONS, ODD-EVEN NUCLEI, ORGANIC CHLORINE COMPOUNDS, ORGANIC COMPOUNDS, ORGANIC HALOGEN COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, ORGANIC SULFUR COMPOUNDS, OXYGEN COMPOUNDS, POLAR SOLVENTS, SOLVENTS, SPECTRA, STABLE ISOTOPES, SULFOXIDES, WATER
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