ラジアレン (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ラジアレン" in Japanese language version.

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  • Iyoda, M., Yamakawa, J. and Rahman, M. J. (2011), Conjugated Macrocycles: Concepts and Applications. Angew. Chem. Int. Ed., 50: 10522–10553. doi:10.1002/anie.201006198
  • Oligomeric and Polymeric Systems with a Cross-conjugated π-Framework Mojtaba Gholami and Rik R. Tykwinski Chemical Reviews 2006 106 (12), 4997-5027 doi:10.1021/cr0505573
  • Hopf, H. and Maas, G. (1992), Preparation and Properties, Reactions, and Applications of Radialenes. Angew. Chem. Int. Ed. Engl., 31: 931–954. doi:10.1002/anie.199209313
  • Effect of Overcrowding in [n]Radialenes on the Synthesis of Bis[4]radialenesMenahem Kaftory, Mark Botoshansky, Shunji Hyoda, Toshihiro Watanabe, and Fumio Toda J. Org. Chem.; 1999; 64(7) pp 2287 - 2292; (Article) doi:10.1021/jo9818
  • Planar [6]Radialenes: Structure, Synthesis, and Aromaticity of Benzotriselenophene and Benzotrithiophene Asit Patra, Yair H. Wijsboom, Linda J. W. Shimon, and Michael Bendikov Angew. Chem. Int. Ed. 2007, 46, 8814 –8818 doi:10.1002/anie.200703123
  • Hopff, H.; Wick, A. K. (1961). “Zur Kenntnis der Hexaalkylbenzole. 3. Mitteilung. Über einen neuen Kohlenwasserstoff C18H24 (Hexaäthylidencyclohexan)”. Helvetica Chimica Acta 44 (2): 380. doi:10.1002/hlca.19610440206. 
  • The Preparation and Properties of Trimethylenecyclopropane Ernest A. Dorko Journal of the American Chemical Society 1965 87 (23), 5518-5520 doi:10.1021/ja00951a067
  • The molecular structure of trimethylenecyclopropane E.A. Dorko , J.L. Hencher, S.H. Bauer Tetrahedron Volume 24, Issue 6, 1968, Pages 2425–2434 doi:10.1016/S0040-4020(01)82515-1
  • Bally, T. and Haselbach, E. (1978), Tris (methylidene)-cyclopropane (“[3]Radialene”). Part 2. Electronic states of the molecular cation and revised UV.-absorption spectrum of the parent neutral. HCA, 61: 754–761. doi:10.1002/hlca.19780610223
  • Synthesis of a Triquinocyclopropane Robert. West and David C. Zecher Journal of the American Chemical Society 1967 89 (1), 152-153 doi:10.1021/ja00977a033
  • Diarylquinocyclopropenes and triquinocyclopropanes Robert West and David C. Zecher Journal of the American Chemical Society 1970 92 (1), 155-161 doi:10.1021/ja00704a025
  • Polyanthraquinocyclopropanes, dianthraquinocyclopropanone, and dianthraquinoethylene. Synthesis and properties Judith L. Benham, Robert West, and John A. T. Norman Journal of the American Chemical Society 1980 102 (15), 5047-5053 doi:10.1021/ja00535a037
  • Negatively substituted trimethylenecyclopropane dianions Tadamichi Fukunaga Journal of the American Chemical Society 1976 98 (2), 610-611 doi:10.1021/ja00418a050
  • Sugimoto, T., Misaki, Y., Kajita, T., Nagatomi, T., Yoshida, Z.-i. and Yamauchi, J. (1988), Tris(thioxanthen-9-ylidene)cyclopropane, and Its Radical Cation and Dication. Angew. Chem. Int. Ed. Engl., 27: 1078–1080. doi: 10.1002/anie.198810781
  • Iyoda, M., Otani, H. and Oda, M. (1988), Tris(fluoren-9-ylidene)cyclopropane, a Novel [3]Radialene. Angew. Chem. Int. Ed. Engl., 27: 1080–1081. doi:10.1002/anie.198810801
  • Lange, T., Gramlich, V., Amrein, W., Diederich, F., Gross, M., Boudon, C. and Gisselbrecht, J.-P. (1995), Hexakis(trimethylsilylethynyl)[3]radialene: A Carbon-Rich Chromophore with Unusual Electronic Properties. Angew. Chem. Int. Ed. Engl., 34: 805–809. doi:10.1002/anie.199508051
  • Miyake, H., Sasamori, T. and Tokitoh, N. (2012), Synthesis and Properties of 4,5,6-Triphospha[3]radialene. Angew. Chem. Int. Ed., 51: 3458–3461. doi:10.1002/anie.201200374
  • The 4,5,6-triphospha[3]radialene dianion: a phosphorus analogue of the deltate dianion. A NICS(0)πzz examination of their aromaticity Hideaki Miyake, Takahiro Sasamori, Judy I-Chia Wu, Paul v. R. Schleyer and Norihiro Tokitoh Chem. Commun., 2012,48, 11440-11442 doi:10.1039/C2CC35978B
  • The first x-ray analysis of a phospha[3]radialene, Polyhedron Volume 11, Issue 3, 1992, Pages 385-387 Ikuko Miyahara, Atsuhiro Hayashi, Ken HirotsuMasaaki Yoshifuji, Hideki Yoshimura, Kozo Toyota doi:10.1016/S0277-5387(00)83187-3
  • Photochemical (E)–(Z) Isomerization of the P=C Double Bond in Triphospha[3]radialene–[M(CO)5] (M = W, Cr) Complexes Takahiro Sasamori, Koki Hirano, Hideaki Miyake, Norihiro Tokitoh Chemistry Letters Vol. 44 (2015) No. 9 P 1240-1242 doi:10.1246/cl.150422
  • Hopf, H. (2012), Phospharadialenes—A New Kid in Town. Angew. Chem. Int. Ed., 51: 11945–11947. doi:10.1002/anie.201206101
  • Triarylamines on [3]Radialene Scaffold: Novel [3]Radialene-based, Multistep, Wide-range Redox Systems with Remarkably Low Oxidation Potentials Kouzou Matsumoto, Nao Yamada, Tetsuya Enomoto, Hiroyuki Kurata, Takeshi Kawase, Masaji Oda Chemistry Letters Vol. 40 (2011) No. 9 P 1033-1035 doi:10.1246/cl.2011.1033
  • The Chemistry of Photodimers of Maleic and Fumaric Acid Derivatives. IV.1 Tetramethylenecyclobutane Gary W. Griffin and Laurence I. Peterson J. Am. Chem. Soc.; 1962; 84(17) pp 3398 - 3400; doi:10.1021/ja00876a033
  • [5]Radialene Emily G. Mackay, Christopher G. Newton, Henry Toombs-Ruane, Erik Jan Lindeboom, Thomas Fallon, Anthony C. Willis, Michael N. Paddon-Row, and Michael S. Sherburn Journal of the American Chemical Society Article ASAP doi:10.1021/jacs.5b07445
  • Barkovich, A. J.; Vollhardt, K. P. C. (1976). “1,5,9-Cyclododecatriyne. Synthesis and conversion to intermediate 1,2:3,4:5,6-tricyclobutabenzene”. Journal of the American Chemical Society 98 (9): 2667. doi:10.1021/ja00425a046. 
  • Harruff, L. G.; Brown, M.; Boekelheide, V. (1978). “Hexaradialene: precursors and structure”. Journal of the American Chemical Society 100 (9): 2893. doi:10.1021/ja00477a055. 
  • Barkovich, A. J.; Strauss, E. S.; Vollhardt, K. P. C. (1977). “Hexaradialene”. Journal of the American Chemical Society 99 (25): 8321. doi:10.1021/ja00467a036. 
  • Schiess, P.; Heitzmann, M. (1978). “Hexakis (methylidene)-cyclohexane (?[6]Radialene?). Chemical and spectral properties”. Helvetica Chimica Acta 61 (2): 844. doi:10.1002/hlca.19780610232. 
  • Hopff, H.; Wick, A. K. (1961). “Zur Kenntnis der Hexaalkylbenzole. 2. Mitteilung. Seitenkettenhalogenierungen von Hexaäthylbenzol”. Helvetica Chimica Acta 44 (1): 19. doi:10.1002/hlca.19610440104. 
  • Iyoda, M.; Tanaka, S.; Otani, H.; Nose, M.; Oda, M. (1988). “A new approach to the construction of radialenes by the nickel-catalyzed cyclooligomerization of [3]cumulenes (butatrienes)”. Journal of the American Chemical Society 110 (25): 8494. doi:10.1021/ja00233a028. 
  • Stanger, A.; Ashkenazi, N.; Boese, R.; Bläser, D.; Stellberg, P. (1997). “Hexabromotricyclobutabenzene and Hexabromohexaradialene: Their Nickel-Mediated One-Pot Syntheses and Crystal Structure”. Chemistry: A European Journal 3 (2): 208. doi:10.1002/chem.19970030207. 
  • Shinozaki, S.; Hamura, T.; Ibusuki, Y.; Fujii, K.; Uekusa, H.; Suzuki, K. (2010). “Hexaradialenes by Successive Ring Openings of Tris(alkoxy-tricyclobutabenzenes): Synthesis and Characterization”. Angewandte Chemie International Edition in English 49 (17): 3026–3029. doi:10.1002/anie.200907305. PMID 20333636. 
  • Synthesis and Diels–Alder Reactions of a Benzo[5]radialene Derivative Andreas A. von Richthofen, Liliana Marzorati, Lucas C. Ducati, and Claudio Di Vitta Organic Letters 2014 16 (15), 4020-4023 doi:10.1021/ol5018432
  • Januszewski, J. A., Hampel, F., Neiss, C., Görling, A. and Tykwinski, R. R. (2014), Unexpected Formation of a [4]Radialene and Dendralenes by Addition of Tetracyanoethylene to a Tetraaryl[5]cumulene. Angew. Chem. Int. Ed., 53: 3743–3747. doi:10.1002/anie.201309355
  • 2-D Coordination Polymers of Hexa(4-cyanophenyl)[3]-radialene and Silver(I): Anion···π-Interactions and Radialene C−H···Anion Hydrogen Bonds in the Solid-State Interactions of Hexaaryl[3]-radialenes with Anions Courtney A. Hollis, Lyall R. Hanton, Jonathan C. Morris, and Christopher J. Sumby Crystal Growth & Design 2009 9 (6), 2911-2916 doi:10.1021/cg9002302
  • Two-Dimensional and Three-Dimensional Coordination Polymers of Hexakis(4-cyanophenyl)[3]radialene: The Role of Stoichiometry and Kinetics Courtney A. Hollis, Stuart R. Batten, and Christopher J. Sumby Crystal Growth & Design 2013 13 (6), 2350-2361 doi:10.1021/cg400036x

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pubmed.ncbi.nlm.nih.gov

  • Shinozaki, S.; Hamura, T.; Ibusuki, Y.; Fujii, K.; Uekusa, H.; Suzuki, K. (2010). “Hexaradialenes by Successive Ring Openings of Tris(alkoxy-tricyclobutabenzenes): Synthesis and Characterization”. Angewandte Chemie International Edition in English 49 (17): 3026–3029. doi:10.1002/anie.200907305. PMID 20333636.