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2-ピリドン (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "2-ピリドン" in Japanese language version.

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21doi.org
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3nih.gov
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1arkat-usa.org
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1wiley.com
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1archive.is
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1scijournals.org
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1anl.gov
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1asm.org
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anl.gov

mesg.anl.gov

archive.is

arkat-usa.org

asm.org

aem.asm.org

doi.org

  • Yang H. W., Craven B. M. (1998). “Charge Density of 2-Pyridone”. Acta Crystallogr. B 54: 912–920. doi:10.1107/S0108768198006545. PMID 9880899. 
  • Penfold B. R. (1953). “The Electron Distribution in Crystalline Alpha Pyridone”. Acta Crystallogr. 6: 591–600. doi:10.1107/S0365110X5300168X. 
  • Almlöf J., Kvick A., Olovsson I. (1971). “Hydrogen Bond Studies Crystal Structure of Intermolecular Complex 2-Pyridone-6-Chloro-2-Hdroxypyridine”. Acta Crystallogr. B 27: 1201–1208. doi:10.1107/S0567740871003753. 
  • Vögeli U., von Philipsborn W. (1973). “C-13 and H-1 NMR Spectroscopie Studies on Structure of N-Methyle-3-Pyridone and 3-Hydroypyridine”. Org Magn Reson 5: 551–559. doi:10.1002/mrc.1270051202. 
  • Leis D. G., Curran B. C. (1945). “Electric Moments of Some Gamma-Substituted Pyridines”. Journal of the American Chemical Society 67 (67): 79–81. doi:10.1021/ja01217a028. 
  • Albert A., Phillips J. N. (1956). “Ionisation Constants of Heterocyclic Substances Hydroxy-Derivates of Nitrogenous Six-Membered Ring-Compounds”. J. Chem. Soc.: 1294–1304. doi:10.1039/jr9560001294. 
  • Cox R. H., Bothner-By A. A (1969). “Proton Magnetic Resonance Spectra of Tautomeric Substituted Pyridines and Their Conjugated Acides”. J. Phys. Chem. 73 (73): 2465–2468. doi:10.1021/j100842a001. 
  • Aksnes DW, Kryvi; Kryvi, Håkon; Samuelson, Olof; Sjöstrand, Elisabeth; Svensson, Sigfrid (1972). “Substituent and Solvent Effects in Proton Magnetic -Resonance (PMR) Spectra of 6 2-Substituted Pyridines”. Acta. Chem. Scand. 26 (26): 2255–2266. doi:10.3891/acta.chem.scand.26-2255. 
  • Aue DH, Betowski LD, Davidson WR, Bower MT, Beak P (1979). “Gas-Phase Basicities of Amides and Imidates - Estimation of Protomeric Equilibrium-Constantes by the Basicity methode in the Gas-Phase”. Journal of the American Chemical Society 101 (101): 1361–1368. doi:10.1021/ja00500a001. 
  • Frank J., Alan R. Katritzky (1976). “Tautomeric pyridines. XV. Pyridone-hydroxypyridine equilibria in solvents of different polarity”. J Chem Soc Perkin Trans 2: 1428–1431. doi:10.1039/p29760001428. 
  • Brown R. S., Tse A., Vederas J. C. (1980). “Photoelectro-Determined Core Binding Energies and Predicted Gas-Phase Basicities for the 2-Hydroxypyridine 2-Pyridone System”. Journal of the American Chemical Society 102 (102): 1174–1176. doi:10.1021/ja00523a050. 
  • Beak P. (1977). “Energies and Alkylation of Tautomeric Heterocyclic-Compounds - Old Problems New Answers”. Acc. Chem. Res. 10 (10): 186–192. doi:10.1021/ar50113a006. 
  • Abdulla H. I., El-Bermani M. F. (2001). “Infrared studies of tautomerism in 2-hydroxypyridine 2-thiopyridine and 2-aminopyridine”. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 57 (57): 2659–2671. doi:10.1016/S1386-1425(01)00455-3. 
  • Hammes GG, Lillford PJ (1970). “A Kinetic and Equilibrium Study of Hydrogen Bond Dimerization of 2-Pyridone in Hydrogen Bonding Solvent”. J. Am. Chem. Soc. 92 (92): 7578–7585. doi:10.1021/ja00729a012. 
  • Rybakov V. R., Bush A. A., Babaev E. B., Aslanov L. A. (2004). “3-Cyano-4,6-dimethyl-2-pyridone (Guareschi Pyridone)”. Acta Crystallogr E 6: o160-o161. doi:10.1107/S1600536803029295. 
  • Fischer C. B., Steininger H., Stephenson D. S., Zipse H. (2005). “Catalysis of Aminolysis of 4-Nitrophenyl Acetate by 2-Pyridone”. Journal for Physical Organic Chemistry 18 (9): 901–907. doi:10.1002/poc.914. 
  • Rawson J. M., Winpenny R. E. P. (1995). “The coordination chemistry of 2-pyridones and its derivatives”. Coordination Chemistry Reviews 139 (139): 313–374. doi:10.1016/0010-8545(94)01117-T. 
  • Sims, Gerald K.; S (1985). “Degradation of Pyridine Derivatives in Soil”. Journal of Environmental Quality 14 (4): 580–584. doi:10.2134/jeq1985.00472425001400040022x. オリジナルの2008年08月30日時点におけるアーカイブ。. https://archive.is/20080830100452/http://jeq.scijournals.org/cgi/content/abstract/14/4/580. 
  • Ensign, Jerald C.; Rittenberg, Sydney C. (1963). “A crystalline pigment produced from 2-hydroxypyridine by arthrobacter crystallopoietes n.sp.”. Archives of Microbiology 47: 137–153. doi:10.1007/BF00422519. 
  • Sims, G. K.; O'Loughlin, E.J.; Crawford, Ronald (1989). “Degradation of pyridines in the environment”. CRC Critical Reviews in Environmental Control 19 (4): 309–340. doi:10.1080/10643388909388372. http://www.mesg.anl.gov/Ed_web_files/oloughlinPDF_Files/CREC1989.pdf. 
  • Oloughlin, E; Kehrmeyer, S; Sims, G (1996). “Isolation, characterization, and substrate utilization of a quinoline-degrading bacterium”. International Biodeterioration & Biodegradation 38: 107–118. doi:10.1016/S0964-8305(96)00032-7. 

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Yang H. W., Craven B. M. (1998). “Charge Density of 2-Pyridone”. Acta Crystallogr. B 54: 912–920. doi:10.1107/S0108768198006545. PMID 9880899. 
  • Sims, Gerald K.; O (1992). “Riboflavin Production during Growth of Micrococcus luteus on Pyridine”. Applied and Environmental Microbiology 58 (10): 3423–3425. PMC 183117. PMID 16348793. http://aem.asm.org/cgi/content/abstract/58/10/3423. 

ncbi.nlm.nih.gov

scijournals.org

jeq.scijournals.org

wiley.com

www3.interscience.wiley.com

znaturforsch.com