Carbon-13 NMR study of isoxazolopyridine systems
Author:
Publisher
Wiley
Subject
General Materials Science,General Chemistry,General Materials Science,General Chemistry
Reference16 articles.
1. 13C nuclear magnetic resonance studies on some substituted isoxazoles
2. Carbon-13, proton spin–spin coupling constants in some 4-substituted isothiazoles and related heterocyclics
3. and Interpretation of Carbon-13 NMR Spectra, p. 86. Heyden, London (1976), and references cited therein.
4. The kinetics of the reaction of some chloroisoxazolo[4.5-c] and [5,4-b] pyridines with methoxide ion
5. and J. Chem. Soc., Perkin Trans. 1 in press.
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1. Heterocycles Condensed to the Isoxazole Ring;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
2. Characterization and differentiation of heterocyclic isomers. tandem mass spectrometry and molecular orbital calculations on 3-methylisoxazolo- and 2-methyloxazolopyridines;Journal of the American Society for Mass Spectrometry;1995-10-01
3. [2+4] Cycloaddition reactions of 4-Nitro-3-phenylisoxazole with Carbo- and heterodienes;Tetrahedron;1995-06
4. Carbon-13 NMR studies on azolopyridines. 3—the isothiazolopyridine systems;Magnetic Resonance in Chemistry;1994-04
5. Chemistry of substituted pyrazolo[1,5-a]pyrimidines. Part 4. A structural correction of a series of pyrazolo[5′,1′ : 2,3]pyrimido[5,4-d][1,2]diazepines on the basis of NMR spectroscopy and X-ray diffraction analysis;J. Chem. Soc., Perkin Trans. 2;1994
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