Relevant bibliographies by topics / Pyridinethione

Academic literature on the topic 'Pyridinethione'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Pyridinethione"

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Nowak, Maciej J., Leszek Lapinski, Hanna Rostkowska, Andrzej Les, and Ludwik Adamowicz. "Theoretical and matrix-isolation experimental study on 2(1H)-pyridinethione/2-pyridinethiol." Journal of Physical Chemistry 94, no. 19 (September 1990): 7406–14. http://dx.doi.org/10.1021/j100382a018.

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Moran, Damian, Kengkaj Sukcharoenphon, Ralph Puchta, Henry F. Schaefer, Paul v. R. Schleyer, and Carl D. Hoff. "2-Pyridinethiol/2-Pyridinethione Tautomeric Equilibrium. A Comparative Experimental and Computational Study." Journal of Organic Chemistry 67, no. 25 (December 2002): 9061–69. http://dx.doi.org/10.1021/jo0263768.

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NOWAK, M. J., L. LAPINSKI, H. ROSTKOWSKA, A. LES, and L. ADAMOWICZ. "ChemInform Abstract: Theoretical and Matrix-Isolation Experimental Study on 2(1H)- Pyridinethione/2-Pyridinethiol." ChemInform 22, no. 1 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199101078.

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Bond, A., and W. Jones. "1-Hydroxy-2(1H)-pyridinethione." Acta Crystallographica Section C Crystal Structure Communications 55, no. 9 (September 15, 1999): 1536–38. http://dx.doi.org/10.1107/s0108270199006824.

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Xu, Xiaojia, Hao Zhang, Erpeng Li, Pengbin Ru, Han Chen, Zhenhua Chen, Yongzhen Wu, He Tian, and Wei-Hong Zhu. "Electron-enriched thione enables strong Pb–S interaction for stabilizing high quality CsPbI3 perovskite films with low-temperature processing." Chemical Science 11, no. 12 (2020): 3132–40. http://dx.doi.org/10.1039/c9sc06574a.

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Zayed, Salem E., Eiman I. Abou Elmaged, Saud A. Metwally, and Mohamed H. Elnagdi. "Reactions of six-membered heterocyclic β-enaminonitriles with electrophilic reagents." Collection of Czechoslovak Chemical Communications 56, no. 10 (1991): 2175–82. http://dx.doi.org/10.1135/cccc19912175.

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The nitriles I reacted with acetylacetone and with ethyl acetoacetate to afford 2-amino-3-cyano-4H-pyran derivatives. They reacted further to yield pyranopyridine derivatives. The reaction of V with acetylacetone afforded the pyridinethione VIII. This afforded, reacting with aromatic aldehydes or with cinnamonitriles quinoline derivatives XVII.
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Sanmartin, J., M. R. Bermejo, J. Romero, J. A. García-Váquez, A. Sousa, A. Brodbeck, A. Castiñeiras, W. Hiller, and J. Strähle. "Electrochemical Synthesis of N-Oxopyridine-2-thionate Complexes of Cd(II): The Crystal Structure of Bis(2,2′-bipyridine)(N-oxopyridine-2-thionate) Cadmium(II) Perchlorate 1/4 (Bipyridine)." Zeitschrift für Naturforschung B 48, no. 4 (April 1, 1993): 431–37. http://dx.doi.org/10.1515/znb-1993-0406.

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The electrochemical oxidation of Cd in acetonitrile solution of 1-hydroxy-2-pyridinethione (HPT) and 2,2′-bipyridine (bipy) affords [Cd(PT)2(bipy)] · H2O and [Cd(PT)(bipy)2]ClO4· 1/4(bipy). The crystal structure of the perchlorate salt shows the molecule to have a distorted octahedral CdN4OS skeleton.
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Elgemeie, Galal E. H., and Adel M. E. Attia. "Novel Synthesis of Condensed Pyridinethione Carbocyclic Glycosides." Phosphorus, Sulfur, and Silicon and the Related Elements 92, no. 1-4 (July 1994): 95–99. http://dx.doi.org/10.1080/10426509408021461.

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Elgemeie, Galal E. H., Adel M. E. Attia, Ali M. Elzanate, and A. K. Mansour. "Convenient Synthesis of 2(1H)-Pyridinethione Glycosides." Bulletin of the Chemical Society of Japan 67, no. 6 (June 1994): 1627–32. http://dx.doi.org/10.1246/bcsj.67.1627.

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SAKURAI, Tadamitsu, Nobuhiro ADACHI, and Hiroyasu INOUE. "Photodimerization reaction of 1-hydroxy-2-pyridinethione." NIPPON KAGAKU KAISHI, no. 5 (1988): 831–34. http://dx.doi.org/10.1246/nikkashi.1988.831.

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Dissertations / Theses on the topic "Pyridinethione"

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Bridon, Dominique. "Application des réactions radicalaires en synthèse organique." Paris 11, 1986. http://www.theses.fr/1986PA112329.

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Les anhydrides mixtes des acides carboxyliques et de la N-oxyde-pvridinethione-2, subissent une réaction de décarboxylation par l'intermédiaire d'un mécanisme radicalaire en chaîne produisant ainsi des radicaux carbonés. La compréhension du mécanisme, et la reconnaissance de l'importance de la température pendant la réaction ont contribué à l'amélioration sensible de la maitrise du système de décarboxylation. Le piégeage des radicaux par des composes diséléniés ou ditellurés a conduit à la formation de nor-alkylséléniures t nor-alkyltellures avec d'excellents rendements. La réaction des radicaux sur les quinones a permis d'obtenir facilement des quinones alkylées. L'addition de radicaux sur les composés de la colonne Vb de la classification périodique a permis de trouver une nouvelle méthode de phosphorylation, ainsi qu’une méthode efficace de transformation des acides carboxyliques en nor-alcools par l'intermédiaire d’un dérivé de l’antimoine
Mixed anhydrides of 2-mercapto-pyridine-N-oxyde carboxylic acids undergo a decarboxylation reaction via a chain mechanism which produces carbon radicals. A real improvement in the control of the system of decarboxylation has been obtained by the mechanism understanding and the recognition of the major role of temperature during the reaction. Radical trapping with diselenide results in the formation of nor-selenide or nor-telluride with high yields. The radical reaction on quinones enabled us to obtain alkyl quinones easily. Addition of radicals to compounds of the Vb column of the periodic classification leads to find a new reaction of phosphorylation, as well as a method of transforming carboxylic acids into nor-alcohol through an antimony derivative
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Harman, David Grant, and harmandg@hotmail com. "Mechanisms of the Intriguing Rearrangements of Activated Organic Species." The Australian National University. Faculty of Science, 2003. http://thesis.anu.edu.au./public/adt-ANU20031210.143110.

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The β-acyloxyalkyl radical rearrangement has been known since 1967 but its mechanism is still not fully understood, despite considerable investigation. Since the migration of a β-trifluoroacetoxy group generally proceeds more rapidly and with more varied regiochemistry than its less electronegative counterparts, this reaction was studied in the hope of understanding more about the subtleties of the mechanism of the β- acyloxyalkyl radical rearrangement. The mechanism of the catalysed rearrangement of Nalkoxy- 2(1H)-pyridinethiones was also explored because preliminary studies indicated that the transition state (TS) for this process was isoelectronic with TSs postulated for the β-acyloxyalkyl radical and other novel rearrangements. ¶ A kinetic study of the rearrangement of the 2-methyl-2-trifluoroacetoxy-1-heptyl radical in solvents of different polarity was undertaken using a radical clock method. Arrhenius equations for the rearrangement in each solvent were: hexane, log10[kr (s-1)] = 11.8±0.3 – (48.9±0.7)/ θ; benzene, log10[kr (s-1)] = 12.0±0.2 – (43.7±0.8)/ θ; and propionitrile, log10[kr (s-1)] = 11.9±0.2 – (42.0±0.3)/ θ. Rate constants at 75˚C were: hexane, kr = 2.9 × 104; benzene, kr = 2.8 × 105; and propionitrile, kr = 4.0 × 105 s-1. The equilibrium constant for the reversible rearrangement at 80°C in benzene was 15.1
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Books on the topic "Pyridinethione"

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Becher, J. Recent Developments in the Synthesis and Chemistry of 2 (1H)-Pyridinethiones and Related Compounds. Routledge, 1988.

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Book chapters on the topic "Pyridinethione"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with methyl substituted 1-hydroxy-2(1H)-pyridinethione." In Magnetic Properties of Paramagnetic Compounds, 425–26. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_223.

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Spitzner, D. "Oxidative Aromatization of Pyridinethiones." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00362.

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Spitzner, D. "S-Alkylation or S-Acylation of N-Substituted Pyridinethiones." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00524.

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Spitzner, D. "Aromatization of Pyridinones and Pyridinethiones by Alkylation, Acylation, or Silylation." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00361.

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You might also be interested in the extended bibliographies on the topic 'Pyridinethione' for particular source types:
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