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Collect. Czech. Chem. Commun. 1959, 24, 1602-1607
https://doi.org/10.1135/cccc19591602

Note on the mass spectra of alkylthiophenes, and the structure of the ion C5H5S+

V. Hanuš and V. Čermák

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  • Reus Christian, Guo Fang, John Alexandra, Winhold Marcel, Lerner Hans-Wolfram, Jäkle Frieder, Wagner Matthias: Air- and Water-Stable, Fluorescent Oligomers of 9,10-Dihydro-9,10-diboraanthracene. Macromolecules 2014, 47, 3727. <https://doi.org/10.1021/ma500518x>
  • Curtis M. David, McClain Mark D.: A New Poly(3-alkylthiophene) Synthesis via Pd-Catalyzed Coupling of Thienyl Mercuric Chlorides. Chem. Mater. 1996, 8, 936. <https://doi.org/10.1021/cm9505308>
  • Gozzo Fabio Cesar, Eberlin Marcos N.: The ionized methylene transfer from the distonic radical cation +CH2-O-CH2 to heterocyclic compounds. A pentaquadrupole mass spectrometric study. J. Am. Soc. Mass Spectrom. 1995, 6, 554. <https://doi.org/10.1016/1044-0305(95)00246-A>
  • Lange D., Budzikiewicz H.: Side‐chain effects on the fragmentation behaviour of alkylthiophenes. Org. Mass Spectrom. 1994, 29, 432. <https://doi.org/10.1002/oms.1210290807>
  • Jagodziński Tadeusz: Mass spectra of some 2‐thiophenecarbothioamides. Org. Mass Spectrom. 1988, 23, 151. <https://doi.org/10.1002/oms.1210230216>
  • Fisichella Salvatore, Occhipinti Salvatore, Arnone Caterina, Consiglio Giovanni, Spinelli Domenico, Noto Renato: Mass spectra of some 2‐ and 4‐substituted thiophenecarboxylic acids. Org. Mass Spectrom. 1983, 18, 449. <https://doi.org/10.1002/oms.1210181009>
  • Fisichella S., Occhipinti S., Consiglio O., Spinelli D., Noto R.: THE MASS SPECTRA OF SOME SUBSTITUTED THIOPHENE-2-CARBOXYLIC ACIDS. Phosphorus and Sulfur and the Related Elements 1982, 13, 59. <https://doi.org/10.1080/03086648208078982>
  • Fisichella Salvatore, Occhipinti Salvatore, Alberghina Gaetano, Amato Maria Emanuela: The mass spectra of some substituted thiophene‐2‐carboxanilides. Journal of Heterocyclic Chem 1981, 18, 1011. <https://doi.org/10.1002/jhet.5570180532>
  • Occhipinti Salvatore, Alberghina Gaetano, Fisichella Salvatore, Puglisi Orazio, Ceraulo Leopoldo: The fragmentation of 5‐ and 3‐substituted thiophene‐2‐carboxamides under electron impact. Org. Mass Spectrom. 1980, 15, 632. <https://doi.org/10.1002/oms.1210151207>
  • El-borai M., Abdel-megeed M. F.: MASS SPECTRAL FRAGMENTATION STUDIES ON THIOPHENOTROPONE AND THIOPHENOTROPILIDENE DERIVATIVES AND THEIR METAL TRICARBONYL COMPLEXS. Phosphorus and Sulfur and the Related Elements 1980, 9, 165. <https://doi.org/10.1080/03086648008078235>
  • Srinivasan M., Rampal J. B., Thiagarajan S.: ELECTRON IMPACT STUDIES ON NITROAROYLTHIOPHENES. Phosphorus and Sulfur and the Related Elements 1977, 3, 221. <https://doi.org/10.1080/03086647708077716>
  • Trofimov B. A., Kalabin G. A., Kryuchkov V. V., Keiko V. V., Amosova S. V., Bzhezovskii V. M., Voronov V. K., Kushnarev D. F., Vitkovskii V. Yu., Lavlinskaya L. I., Pestunovich V. A.: Synthesis of 2-thiabicyclo[3.2.0]hept-3-enes by reaction of acetylene with sodium sulfide. Chem Heterocycl Compd 1976, 12, 745. <https://doi.org/10.1007/BF00477002>
  • Grayshan P. H., Mak K. H. R., Peters Arnold T.: New dyestuffs for synthetic fibres, benzimidazo‐thioxantheno‐isoquinolin‐ones. J. Appl. Chem. 1974, 24, 121. <https://doi.org/10.1002/jctb.2720240304>
  • Grayshan P. H., Mak K. H. R., Peters Arnold T.: New dyestuffs for synthetic fibres, benzimidazo-thioxantheno-isoquinolin-ones. J. Appl. Chem. 1974, 24, 121. <https://doi.org/10.1002/jctb.5020240304>
  • Hirano S., Hiyama T., Fujita S., Kawaguti T., Hayashi Y., Nozaki H.: The syntheses and conformational studies of [n](2,4)heterophanes and [7](3,5)pyrazolophane. Tetrahedron 1974, 30, 2633. <https://doi.org/10.1016/S0040-4020(01)97422-8>
  • Wakkers P. J. M., Janssen Matthijs J., Weringa W. D.: Ring expansion and hydrogen scrambling in the molecular ion of 3‐methylthiophene. Org. Mass Spectrom. 1972, 6, 963. <https://doi.org/10.1002/oms.1210060905>
  • Flores S. E., Vélez M., Rivas C.: Mass spectra of photoaddition products from methyl‐substituted maleic anhydrides and thiophen derivatives. Org. Mass Spectrom. 1971, 5, 1049. <https://doi.org/10.1002/oms.1210050904>
  • Fujita Shinsaku, Kawaguti Takeyuki, Nozaki Hitosi: Synthesis of [6] (2,4)heterophanes. Tetrahedron Letters 1971, 12, 1119. <https://doi.org/10.1016/S0040-4039(01)96642-0>
  • Buu‐Hoï N. P., Croisy A., Jacquignon P., Martani A., Ricci A.: The mass spectra of pseudo‐azulenes containing both nitrogen‐ and sulfur‐heteroatoms. Journal of Heterocyclic Chem 1970, 7, 931. <https://doi.org/10.1002/jhet.5570070430>
  • Pedersen A.O., Schroll G., Lawesson S.-O., Laurie W.A., Reed R.I.: o-Hydroxyphenyl alkyl sulphides, -sulphoxides, and -sulphones. Tetrahedron 1970, 26, 4449. <https://doi.org/10.1016/S0040-4020(01)93093-5>
  • Goudie R. S., Preston P. N., Palmer M. H.: The mass spectra of sydnones. Org. Mass Spectrom. 1969, 2, 953. <https://doi.org/10.1002/oms.1210021004>
  • Brooks C. J. W., Middleditch B. S., Anthony G. M.: The mass spectra of some 1,3,2‐oxazaborolidines. Org. Mass Spectrom. 1969, 2, 1023. <https://doi.org/10.1002/oms.1210021011>
  • Foster Norman G., Higgins Robert W.: The mass spectrum of 1‐(2‐thienyl) hexane‐1‐13C. Org. Mass Spectrom. 1968, 1, 191. <https://doi.org/10.1002/oms.1210010202>
  • Naito T.: Studies on isothiazoles—V. Tetrahedron 1968, 24, 6237. <https://doi.org/10.1016/S0040-4020(01)96357-4>
  • Tilak B. D., Das K. G., El-Namaky H. M.: Electron impact studies iv. Expulsion of methylene under electron impact. Experientia 1967, 23, 609. <https://doi.org/10.1007/BF02144148>
  • Grigg R., Sargent M.V., Williams D.H., Knight J.A.: Studies in mass spectroscopy—II. Tetrahedron 1965, 21, 3441. <https://doi.org/10.1016/S0040-4020(01)96967-4>
  • Mayer R., Franke J., Horaák V., Hanker I., Zahradník R.: Synthese und eigenschaften des thialens (cyclopenta-thiapyran). Tetrahedron Letters 1961, 2, 289. <https://doi.org/10.1016/S0040-4039(01)84064-8>
  • Pettit R.: Synthesis of the thiapyrylium cation. Tetrahedron Letters 1960, 1, 11. <https://doi.org/10.1016/S0040-4039(00)70271-1>