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同芳香性 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "同芳香性" in Chinese language version.

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Global rank Chinese rank
27doi.org
2nd place
23rd place
5nih.gov
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2semanticscholar.org
11th place
332nd place
1iupac.org
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562nd place

doi.org

  • International Union of Pure and Applied Chemistry (IUPAC), The IUPAC Compendium of Chemical Terminology，4-th ed. (The Gold Book) (1997)。在線校正版: (2006–) "Homoaromatic"。doi:10.1351/goldbook.H02839
  • Winstein, S. Homo-Aromatic Structures. J. Am. Chem. Soc. 1959, 81 (24): 6523. doi:10.1021/ja01533a052. 
  • Freeman, P. K. Neutral Homoaromaticity in Some Neutral Heterocycles. J. Org. Chem. 2005, 70 (6): 1998–2001. PMID 15760178. doi:10.1021/jo040250o. 
  • Winstein, S.; Sonnenberg, J.; DeVries, L. The Tris-Homocyclopropenyl Cation. J. Am. Chem. Soc. 1959, 81 (24): 6523–6524. doi:10.1021/ja01533a051. 
  • Childs, R. F. The Homotropylium Ion and Homoaromaticity. Acc. Chem. Res. 1984, 17 (10): 347–352. doi:10.1021/ar00106a001. 
  • Hua Yuhui; Zhang Hong; Xia Haiping. History and Development 38 (1): 11–28. 2018. doi:10.6023/cjoc201709009. 
  • Schleyer, P. R. Introduction: Aromaticity. Chem. Rev. 2001, 101 (5): 1115–1118. PMID 11749368. doi:10.1021/cr0103221 可免费查阅. 
  • Rosenburg, J. L.; Mahler, J. E.; Pettit, R. J. The Bicyclo[5.1.0]octadienyl Cation, A New Stable Carbonium Ion. J. Am. Chem. Soc. 1962, 84 (14): 2842–2843. doi:10.1021/ja00873a051. 
  • Winstein, S.; Kaesz, H.D.; Kreiter, C.G.; Friedrich, E.C. Homotropylium Ion and its Molybdenum Tricarbonyl Complex. J. Am. Chem. Soc. 1965, 87 (14): 3267–3269. doi:10.1021/ja01092a060. 
  • Winstein, S.; Kreiter, C.G.; Brauman, J.I. Ring Inversion, Ultraviolet Spectrum, and Electronic Structure of the Monohomotropylium Ion. J. Am. Chem. Soc. 1966, 88 (9): 2047–2048. doi:10.1021/ja00961a037. 
  • Haddon, R.C. The structure of the homotropenylium cation. Tetrahedron Lett. 1975, 16 (11): 863–866. doi:10.1016/S0040-4039(00)72004-1. 
  • Haddon, R.C. Perturbational molecular orbital (PMO) theory of homoaromaticity. J. Am. Chem. Soc. 1975, 97 (13): 3608–3615. doi:10.1021/ja00846a009. 
  • Oth, J.F.M.; Smith, D.M.; Prange, U.; Schröder, G. A [16]Annulenediyl Dication. Angew. Chem. Int. Ed. Engl. 1973, 12 (4): 327–328. doi:10.1002/anie.197303271. 
  • Sal'nikov, G.E.; Genaev, A.M.; Mamatyuk, V.I.; Shubin, V.G. Homophenalenyl cations, new representatives of homoaromatic systems. Russ. J. Org. Chem. 2008, 44 (7): 1000–1005. S2CID 93688550. doi:10.1134/S1070428008070099. 
  • Prinzbach, H.; Gescheidt, G.; Martin, H.-D.; Herges, R.; Heinze, J.; Prakash, G. K. Surya; Olah, G. A. Cyclic electron delocalization in hydrocarbon cages (pagodanes, isopagodanes, (bisseco-/seco-)-(dodecahedradienes)). Pure and Applied Chemistry: 673–682, 1995. S2CID 96232491. doi:10.1351/pac199567050673. 
  • Suzuki, T.; Li, Q.; Khemani, K.C.; Wudl, F. Dihydrofulleroid H3C61: synthesis and properties of the parent fulleroid. J. Am. Chem. Soc. 1992, 114 (18): 7301–7302. doi:10.1021/ja00044a055. 
  • Zimmerman, H. E.; Grunewald, G. L. The Chemistry of Barrelene. III. A Unique Photoisomerization to Semibullvalene. Journal of the American Chemical Society. 1966, 88: 183–184. doi:10.1021/ja00953a045. 
  • Dewar, M.J.S.; Lo, D.H. Ground states of .sigma.-bonded molecules. XIV. Application of energy partitioning to the MINDO/2 method and a study of the Cope rearrangement. J. Am. Chem. Soc. 1971, 93 (26): 7201–7207. doi:10.1021/ja00755a014. 
  • Hoffman, D.; Stohrer, W-D. Cope rearrangement revisited. J. Am. Chem. Soc. 1971, 93 (25): 6941–6948. doi:10.1021/ja00754a042. 
  • Griffiths, P. R.; Pivonka, D. E.; Williams, R. V. The Experimental Realization of a Neutral Homoaromatic Carbocycle. Chemistry: A European Journal. 2011, 17 (33): 9193–9199. PMID 21735493. doi:10.1002/chem.201100025. 
  • Keuter J; Hepp A; Massolle A; Neugebauer J; Mück-Lichtenfeld C; Lips F. Synthesis and Reactivity of a Neutral Homocyclic Silylene. Angew Chem Int Ed Engl. 2022, 61 (5). PMID 34797603. doi:10.1002/anie.202114485. 
  • Steiner, D.; Balzereit, C.; Winkler, H. J. R.; Stamatis, N.; Massa, W.; Berndt, A.; Hofmann, M.; Von Ragué Schleyer, P. Nonclassical 1,2-Diboretanes and 1,2-Diborolanes. Angewandte Chemie International Edition in English. 1994, 33 (22): 2303–2306. doi:10.1002/anie.199423031. 
  • Martin, H.D.; Mayer, B. Proximity Effects in Organic Chemistry?The Photoelectron Spectroscopic Investigation of Non-Bonding and Transannular Interactions. Angew. Chem. Int. Ed. Engl. 1983, 22 (4): 283–314. doi:10.1002/anie.198302831. 
  • Steiner, D.; Winkler, H.; Balzereit, C.; Happel, T.; Hofmann, M.; Subramanian, G.; Schleyer, P.V.R.; Massa, W.; Berndt, A. 1,2-Diboretanides: Homoaromatic 2π-Electron Compounds with High Inversion Barriers. Angew. Chem. Int. Ed. Engl. 1996, 35 (17): 1990–1992. doi:10.1002/anie.199619901. 
  • Exner, K.; Hunkler, D.; Gescheidt, G.; Prinzbach, H. Do Nonclassical, Cyclically Delocalized 4N/5e Radical Anions and 4N/6e Dianions Exist? – One- and Two-Electron Reduction of Proximate, Synperiplanar Bis-Diazenes. Angew. Chem. Int. Ed. Engl. 1998, 37 (13–14): 1910–1913. doi:10.1002/(SICI)1521-3773(19980803)37:13/14<1910::AID-ANIE1910>3.0.CO;2-D. 
  • Exner, K.; Cullmann, O.; Vögtle, M.; Prinzbach, H.; Grossmann, B.; Heinze, J.; Liesum, L.; Bachmann, R.; Schweiger, A.; Gescheidt, G. Cyclic In-Plane Electron Delocalization (σ-Bishomoaromaticity) in 4N/5e Radical Anions and 4N/6e Dianions – Generation, Structures, Properties, Ion-Pairing, and Calculations. J. Am. Chem. Soc. 2000, 122 (43): 10650–10660. doi:10.1021/ja0014943. 
  • Volz, H.; Shin, J. Bicyclo[3.2.1]octa-3,6-dien-2-yl Cation: A Bishomoantiaromate. J. Org. Chem. 2006, 71 (6): 2220–2226. PMID 16526766. doi:10.1021/jo0515125. 

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  • Sal'nikov, G.E.; Genaev, A.M.; Mamatyuk, V.I.; Shubin, V.G. Homophenalenyl cations, new representatives of homoaromatic systems. Russ. J. Org. Chem. 2008, 44 (7): 1000–1005. S2CID 93688550. doi:10.1134/S1070428008070099. 
  • Prinzbach, H.; Gescheidt, G.; Martin, H.-D.; Herges, R.; Heinze, J.; Prakash, G. K. Surya; Olah, G. A. Cyclic electron delocalization in hydrocarbon cages (pagodanes, isopagodanes, (bisseco-/seco-)-(dodecahedradienes)). Pure and Applied Chemistry: 673–682, 1995. S2CID 96232491. doi:10.1351/pac199567050673.