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Volumn 48, Issue 3, 2009, Pages 517-520

Isolation of bicyclopropenylidenes: Derivatives of the smallest member of the fulvalene family

Author keywords

Carbenes; Cyclopropenylidenes; Fulvalenes; Hydration; Strained molecules

Indexed keywords

HYDRATION; MAGNESIUM; SOLID SOLUTIONS;

EID: 58249106946     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200804372     Document Type: Article
Times cited : (10)

References (44)
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    • Although the compound was prepared by Courtot, its structure was ascertained in 1971: H. Prinzbach, Pure Appl. Chem. 1971, 28, 281-329
    • Although the compound was prepared by Courtot, its structure was ascertained in 1971: H. Prinzbach, Pure Appl. Chem. 1971, 28, 281-329.
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    • For recent reviews on fulvalenes, see
    • For recent reviews on fulvalenes, see: B. Halton, Eur. J. Org. Chem. 2005, 3391-3414;
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    • For recent reviews on tetrathiafulvalenes, see: a
    • For recent reviews on tetrathiafulvalenes, see: a) M. Bendikov, F. Wudl, D. F. Perepichka, Chem. Rev. 2004, 104, 4891-4945;
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    • Bendikov, M.1    Wudl, F.2    Perepichka, D.F.3
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    • See also
    • See also: P. Batail, Chem. Rev. 2004, 104, 4887-4890.
    • (2004) Chem. Rev , vol.104 , pp. 4887-4890
    • Batail, P.1
  • 23
    • 0001767966 scopus 로고    scopus 로고
    • It is well recognized that annelation of the cyclopropene ring into an aromatic framework significantly enhances its thermodynamic stability. See for examples: a B. Halton, P. J. Stang, Synlett 1997, 145-158;
    • It is well recognized that annelation of the cyclopropene ring into an aromatic framework significantly enhances its thermodynamic stability. See for examples: a) B. Halton, P. J. Stang, Synlett 1997, 145-158;
  • 24
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    • b) B. Halton, Chem. Rev. 2003, 103, 1327-1370;
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    • Angew. Chem. Int. Ed. 2006, 45, 6652-6655;
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    • CCDC 693680 (6a) and 698793 (7b) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif.
    • CCDC 693680 (6a) and 698793 (7b) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif.
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    • Cyclopropenones are notorious for inducing skin sensitivity and dermatitis
    • Cyclopropenones are notorious for inducing skin sensitivity and dermatitis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.