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Journal articles on the topic 'Pyridinethione'

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Published: 4 June 2021

Last updated: 1 February 2022

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Marjani, Katayoun, Sian C. Davies, Marcus C. Durrant, David L. Hughes, and Nejat Khodamorad. "Di-μ-pyridine-2-thiolato-bis[chloro(triphenylphosphine)copper(I)]." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 10, 2006): m744—m746. http://dx.doi.org/10.1107/s1600536806006672.

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The structure of the title compound, [Cu2(C5H5NS)2Cl2(C18H15P)2], shows two independent molecules, each a dimer bridged through a Cu2S2 rectangular plane involving the two pyridinethione S atoms and lying about a centre of symmetry. The Cu atoms have a distorted tetrahedral geometry. There is intramolecular hydrogen bonding between the pyridinium H atoms and the Cl ligands.

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12

Kokkou, S. C., V. Schramm, and P. Karagiannidis. "Structure of tetrakis[2(1H)-pyridinethione-S]copper(I) perchlorate–2-pyridinethione (1/2), [Cu(C5H5NS)4]ClO4.2(C5H5NS)." Acta Crystallographica Section C Crystal Structure Communications 41, no. 7 (July 15, 1985): 1040–43. http://dx.doi.org/10.1107/s0108270185006503.

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13

Hartung, J., I. Svoboda, and M. T. Duarte. "Hydrogen Bonding in 1-Hydroxy-4(1H)-pyridinethione." Acta Crystallographica Section C Crystal Structure Communications 53, no. 11 (November 15, 1997): 1631–34. http://dx.doi.org/10.1107/s0108270197008834.

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14

Shunmugam, R., and D. N. Sathyanarayana. "13C AND1H NMR STUDY OF COMPLEXES OF 2-PYRIDINETHIONE AND 4-PYRIDINETHIONE WITH Zn(II), Cd(II) AND Hg(II) HALIDES." Journal of Coordination Chemistry 14, no. 1 (May 1985): 27–30. http://dx.doi.org/10.1080/00958978508080674.

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15

Fu, Aiping, Hongliang Li, and Dongmei Du. "Thiol-thione tautomerism in 2-pyridinethione: Effect of hydration." Journal of Molecular Structure: THEOCHEM 767, no. 1-3 (August 2006): 51–60. http://dx.doi.org/10.1016/j.theochem.2006.04.025.

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16

ELGEMEIE, G. E. H., A. M. E. ATTIA, A. M. ELZANATE, and A. K. MANSOUR. "ChemInform Abstract: Convenient Synthesis of 2(1H)-Pyridinethione Glycosides." ChemInform 25, no. 44 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199444216.

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17

Babu Mareyala, Hari. "Addition of 2(1H)-Pyridinethione to 3,4-Dihydro(2H)-pyran." HETEROCYCLES 24, no. 9 (1986): 2403. http://dx.doi.org/10.3987/r-1986-09-2403.

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18

Attia, Adel M. E., Elsayed I. Ibrahim, Fouad E. A. Hay, Mohammed M. A. Abbasi, and Hanaa A. E. Mansour. "NOVEL SYNTHESIS OF SOME PYRIDINETHIONE NUCLEOSIDES RELATED TO 3-DEAZAUREDINE." Organic Preparations and Procedures International 27, no. 6 (December 1995): 613–19. http://dx.doi.org/10.1080/00304949509458518.

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19

Elgemeie, Galal E. H., Adel M. E. Attia, and Nahed M. Fathy. "Novel Synthesis of a New Class of Polynuclear Pyridinethione Nucleosides." Nucleosides and Nucleotides 16, no. 4 (April 1997): 485–93. http://dx.doi.org/10.1080/07328319708001365.

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20

Abdelhamid, Abdou O., and Sobhi M. Gomha. "Synthesis of New Pyrazolo[1,5-a]pyrimidine, Triazolo[4,3-a]pyrimidine Derivatives, and Thieno[2,3-b]pyridine Derivatives from Sodium 3-(5-Methyl-1-phenyl-1H-pyrazol-4-yl)-3-oxoprop-1-en-1-olate." Journal of Chemistry 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/327095.

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Condensation of sodium 3-oxo-3-(1-phenyl-1H-pyrazol-4-yl)prop-1-en-1-olate (2) with several heterocyclic amines, cyanoacetamide, cyanothioacetamide, and 2-cyanoacetohydrazide gives pyrazolo[1,5-a]pyrimidines (5a–d), pyrido[2′,3′:3,4]pyrazolo[1,5-a]pyrimidine (9), benzo[4,5]imidazo[1,2-a]pyrimidine (10), [1,2,4]triazolo[1,5-a]pyrimidine (11), and pyridine derivatives (12–14). Also, thieno[2,3-b]pyridines (15–18) were synthesized via pyridinethione (13) withα-halo ketones andα-halo ester. Structures of the newly synthesized compounds were elucidated by elemental analysis, spectral data, alternative synthetic routes, and chemical transformation whenever possible.

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21

Giusti, G., G. Geier, A. Currao, and R. Nesper. "Thione Compounds of Copper and Silver: Tetrakis[1-methyl-2(1H)-pyridinethione-S]copper(I) Tetrafluoroborate and Tetrakis-[1-methyl-2(1H)-pyridinethione-S]silver(I) Tetrafluoroborate." Acta Crystallographica Section C Crystal Structure Communications 52, no. 8 (August 15, 1996): 1914–17. http://dx.doi.org/10.1107/s0108270196003666.

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22

Becher, Jan, Fahmy M. Asaad, Tea Johansen, Jesper Hansen, Sine Larsen, and Flemming Hansen. "Pyridinethiones. XI. Diastereoselective aldol condensations with 2(1H)-pyridones, 2(1H)-pyridinethiones, and the crystal structure of 3-(1-hydroxy-2-methyl-3-oxo-3-(4-chlorophenyl)propyl-1-isoprpyl-2(1H)-pyridinethione." Journal of Heterocyclic Chemistry 23, no. 2 (March 1986): 567–75. http://dx.doi.org/10.1002/jhet.5570230252.

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23

Boivin, Jean, Elisabeth Crépon (née da Silva), and Samir Z. Zard. "N-hydroxy-2-pyridinethione: A mild and convenient source of hydroxyl radicals." Tetrahedron Letters 31, no. 47 (January 1990): 6869–72. http://dx.doi.org/10.1016/s0040-4039(00)97193-4.

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24

Fathy, Nahed M. "NOVEL SYNTHESIS OF CONDENSED PYRIDINETHIONE NUCLEOSIDES AND CONDENSED THIEN0[2,3-b]PYRIDINES." Phosphorus, Sulfur, and Silicon and the Related Elements 107, no. 1-4 (November 1, 1995): 7–12. http://dx.doi.org/10.1080/10426509508027915.

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25

Abdel Hafez, Ali A., Ibrahim M. A. Awad, and Ragaa A. Ahmed. "Synthesis of Azo-Sulfa Drugs Based on 2-Pyridinone and 2-Pyridinethione." Journal of the Chinese Chemical Society 40, no. 3 (June 1993): 289–96. http://dx.doi.org/10.1002/jccs.199300043.

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26

ATTIA, A. M. E., E. I. IBRAHIM, F. E. A. HAY, M. M. A. ABBASI, and H. A. E. MANSOUR. "ChemInform Abstract: Novel Synthesis of Some Pyridinethione Nucleosides Related to 3- Deazauridine." ChemInform 27, no. 18 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199618234.

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27

Schanck, A., J. M. Dereppe, and M. van Meerssche. "1H And 1 3C NMR of some mercaptopyridine and pyridinethione carboxylic acids." Bulletin des Sociétés Chimiques Belges 92, no. 3 (September 1, 2010): 199–202. http://dx.doi.org/10.1002/bscb.19830920301.

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28

ELGEMEIE, G. E. H., A. M. E. ATTIA, and N. M. FATHY. "ChemInform Abstract: Novel Synthesis of a New Class of Polynuclear Pyridinethione Nucleosides." ChemInform 28, no. 40 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199740277.

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29

Rajalingam, Umarani, Philip AW Dean, and Hilary A. Jenkins. "Solution multinuclear (31P,111Cd,77Se) magnetic resonance studies of cadmium complexes of heterocyclic aromatic thiones and the structure of [tetrakis(2(1H)-pyridinethione)cadmium] nitrate, [Cd(C5H5NS)4](NO3)2." Canadian Journal of Chemistry 78, no. 5 (May 1, 2000): 590–97. http://dx.doi.org/10.1139/v00-070.

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The complex salts CdL4(O3SCF3)2 (L = 2(1H)-pyridinethione (Py2SH), 4(1H)-pyridinethione (Py4SH), or 2(1H)-quinolinethione (Q2SH)) have been synthesized by the stoichiometric reaction of Cd(O3SCF3)2 and the appropriate thione. Both ambient-temperature 13C and reduced-temperature 111Cd NMR of CdL4(O3SCF3)2 in solution are consistent with L being bound through sulfur. Reduced-temperature NMR (31P, 77Se, 111Cd, as appropriate) of mixtures of CdL4(O3SCF3)2 and Cd(EPCy3)4(O3SCF3)2 (E = Se, Cy = c-C6H11) and of Cd(EPCy3)4(O3SCF3)2 (E = S, Se) and L in solution provides evidence for various [CdLn(EPCy3)4-n]2+. Similarly, reduced-temperature metal NMR of [CdL4]2+ and [CdL'4]2+ (L, L' = Py2SH, Py4SH, Q2SH; L not equal L') in solution shows the formation of [CdLnL'4-n]2+. Thus it has been demonstrated that at reduced temperature [CdL4]2+ is intact in solution and exchange of L is slow on the timescale of the metal chemical shift differences. From the NMR studies of Cd(EPCy3)4(O3SCF3)2 (E = S, Se):L mixtures, the binding preferences are found to be L > EPCy3 in solution. Similarly, from the reduced temperature metal NMR spectra of mixtures where L and L' compete for Cd(II) in solution, the binding preferences are Py4SH > Py2SH > Q2SH. The structure of Cd(Py2SH)4(NO3)2 (4) has been determined by single crystal X-ray analysis. Colorless crystals of 4 are tetragonal, I4(1)/acd with 8 molecules per unit cell of dimensions a = 18.660(3), c = 15.215(3) Å. The structure is comprised of recognizable NO3- anions and [Cd(Py2SH)4]2+ cations. In the cations, which have S4 symmetry, the ligands are S-bound. A network of NH···O hydrogen bonds links the cations and anions.Key words: aromatic heterocyclic thiones, cadmium complexes, phosphine chalcogenides, 111Cd, 31P, 77Se NMR, X-ray crystallography.

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30

Elneairy, Mohamed A. A., Sanaa M. Eldin, Fawzy A. Attaby, and Ali K. K. El-louh. "Cyanothioacetamide in Heterocyclic Chemistry: Synthesis of Thiopyran, Pyridinethione, Thienopyridine, Pyridothienotriazine and Pyridothienopyrimidine Derivatives." Phosphorus, Sulfur, and Silicon and the Related Elements 167, no. 1 (January 1, 2000): 289–302. http://dx.doi.org/10.1080/10426500008082407.

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31

Valle, Giovanni, Renato Ettorre, Umberto Vettori, Valerio Peruzzo, and Gualtiero Plazzogna. "Crystal structure and mass spectrometry of dichlorodimethylbis[2(1H)-pyridinethione-S]tin(IV)." Journal of the Chemical Society, Dalton Transactions, no. 4 (1987): 815. http://dx.doi.org/10.1039/dt9870000815.

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32

Giorgi, Gianluca, Laura Salvini, and Fabio Ponticelli. "Hydrolysis of methylthiazolopyridines. X-ray crystal structure of 3-acetamido-2(1H)-pyridinethione." Journal of Heterocyclic Chemistry 37, no. 2 (March 2000): 421–23. http://dx.doi.org/10.1002/jhet.5570370232.

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33

Elgemeie, Galal E. H., Adel M. E. Attia, and Nahed M. Fathy. "Glycosides of Heterocycles: A Direct Route to 1-(β-D-Glycopyranosyl)pyridinethione Nucleosides." Liebigs Annalen der Chemie 1994, no. 9 (September 2, 1994): 955–58. http://dx.doi.org/10.1002/jlac.199419940919.

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34

Schepp, Norman P., Christopher J. M. Green, and Frances L. Cozens. "Non-resonant two-photon photochemistry of a Barton ester, N-phenylacetyloxy-2-pyridinethione." Photochem. Photobiol. Sci. 9, no. 1 (2010): 110–13. http://dx.doi.org/10.1039/b9pp00066f.

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35

Kaigorodova, E. A., L. D. Konyushkin, S. N. Mikhailichenko, V. K. Vasilin, A. V. Sazonov, and V. G. Kul'nevich. "Synthesis and reactions of 3-cyano-6-methoxymethyl-4-methyl-2(1H)-pyridinethione." Chemistry of Heterocyclic Compounds 35, no. 3 (March 1999): 293–96. http://dx.doi.org/10.1007/bf02259358.

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36

Jasim, Suhair, and Hans Tjälve. "Effect of Zinc Pyridinethione on the Tissue Disposition of Nickel and Cadmium in Mice." Acta Pharmacologica et Toxicologica 59, no. 3 (March 13, 2009): 204–8. http://dx.doi.org/10.1111/j.1600-0773.1986.tb00155.x.

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37

Elgemeie, Galal E. H., Adel M. E. Attia, Dalia S. Farag, and Sherif M. Sherif. "Nucleotides and nucleosides: direct route to condensed pyridinethione carbocyclic nucleosides related to 3-deazauridine." Journal of the Chemical Society, Perkin Transactions 1, no. 10 (1994): 1285. http://dx.doi.org/10.1039/p19940001285.

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38

BOIVIN, J., E. CREPON, and S. Z. ZARD. "ChemInform Abstract: N-Hydroxy-2-pyridinethione: A Mild and Convenient Source of Hydroxyl Radicals." ChemInform 23, no. 8 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199208227.

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39

AHMED, G. A. "ChemInform Abstract: Some Reactions of 3-Cyano-4,6-dimethyl-2(1H)pyridinethione. Part 2." ChemInform 28, no. 4 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199704158.

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40

Shanazarov, A. K., and V. G. Granik. "Reaction of diendiaminodiketones with nucleophilic reagents. Synthesis of 2-pyridone and 2-pyridinethione derivatives." Chemistry of Heterocyclic Compounds 23, no. 3 (March 1987): 359–60. http://dx.doi.org/10.1007/bf00762005.

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41

Povey, D. C., G. W. Smith, T. S. Lobana, and P. K. Bhatia. "X-ray crystal and molecular structure of dichlorobis [2(1H)-pyridinethione-S]iron(II)." Journal of Crystallographic and Spectroscopic Research 21, no. 1 (February 1991): 9–12. http://dx.doi.org/10.1007/bf01158967.

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42

Casella, Luigi, Michele Gullotti, and Roberto Viganò. "Copper(II)-N2S2 complexes of the imines of 1-phenyl-3-formyl-2(1H)-pyridinethione." Inorganica Chimica Acta 124, no. 3 (July 1986): 121–25. http://dx.doi.org/10.1016/s0020-1693(00)85860-0.

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43

Kaigorodova, E. A., L. D. Konyushkin, S. N. Mikhailichenko, V. K. Vasilin, A. V. Sazonov, and V. G. Kul'nevich. "ChemInform Abstract: Synthesis and Reactions of 3-Cyano-6-methoxymethyl-4-methyl-2(1H)-pyridinethione." ChemInform 31, no. 8 (June 10, 2010): no. http://dx.doi.org/10.1002/chin.200008157.

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44

ELGEMEIE, G. E. H., A. M. E. ATTIA, and N. M. FATHY. "ChemInform Abstract: Glycosides of Heterocycles: A Direct Route to 1-(β-D- Glycopyranosyl)pyridinethione Nucleosides." ChemInform 26, no. 6 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199506243.

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45

Sayed, N. I. Abdel. "Spectrophotometric and Conductometric Studies of Charge Transfer Interaction of 2-(1H)-Pyridinethione with π-Acceptors." Journal of the Chinese Chemical Society 50, no. 3A (June 2003): 345–52. http://dx.doi.org/10.1002/jccs.200300052.

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46

Giorgi, Gianluca, Laura Salvini, and Fabio Ponticelli. "ChemInform Abstract: Hydrolysis of Methylthiazolopyridines. X-Ray Crystal Structure of 3-Acetamido-2(1H)-pyridinethione." ChemInform 31, no. 38 (September 19, 2000): no. http://dx.doi.org/10.1002/chin.200038036.

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47

Hussein, Abdel Haleem Mostafa, Fathi Ali Abu-Shanab, and Sayed Abdel Hamed Sayed Mousa. "Benzoylacetone as a Building Block in Heterocyclic Synthesis: Synthesis of Polyfunctionally Substituted Pyridinethione and Its Derivatives." OALib 02, no. 01 (2015): 1–9. http://dx.doi.org/10.4236/oalib.1101274.

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48

ELGEMEIE, G. E. H., A. M. E. ATTIA, D. S. FARAG, and S. M. SHERIF. "ChemInform Abstract: Nucleotides and Nucleosides: Direct Route to Condensed Pyridinethione Carbocyclic Nucleosides Related to 3-Deazauridine." ChemInform 25, no. 38 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199438271.

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49

Lobana, Tarlok S., Paramjit K. Bhatia, and Edward R. T. Tiekink. "Synthesis and X-ray crystal structure of chloro[2(1H)-pyridinethione-S]-bis(triphenylphosphine)copper(I)." Journal of the Chemical Society, Dalton Transactions, no. 4 (1989): 749. http://dx.doi.org/10.1039/dt9890000749.

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50

Jordan, Frank, Zbigniew Kudzin, Zbigniew Witczak, and Philip Hoops. "Nuclear magnetic resonance determination of the site of acylation of the tautomeric nucleophile 4(1H)-pyridinethione." Journal of Organic Chemistry 51, no. 4 (February 1986): 571–73. http://dx.doi.org/10.1021/jo00354a039.

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