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Volumn 47, Issue 28, 2008, Pages 5198-5202

Transformation of a 1-zirconacyclopent-3-yne, a five-membered cycloalkyne, into a 1-zirconacyclopent-3-ene and formal "1-zirconacyclopenta-2,3-dienes

Author keywords

Alkali metals; Alkynes; Allenes; Cyclopentynes; Zirconium

Indexed keywords

ACETYLENE; ALKALI METALS; ALKALINITY; CHEMICAL REACTIONS; HYDROCARBONS; LIGHT METALS; MATHEMATICAL TRANSFORMATIONS; OLEFINS; ZIRCONIUM COMPOUNDS;

EID: 53349097805     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200800739     Document Type: Article
Times cited : (59)

References (69)
  • 5
    • 0002073050 scopus 로고
    • Eds, P. J. Stang, F. Diederich, VCH, Weinheim, chap. 8, pp
    • d) R. Gleiter, R. Merger in Modern Acetylene Chemistry (Eds.: P. J. Stang, F. Diederich), VCH, Weinheim, 1995, chap. 8, pp. 285-317.
    • (1995) Modern Acetylene Chemistry , pp. 285-317
    • Gleiter, R.1    Merger, R.2
  • 22
  • 26
    • 4544224726 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3882-3887.
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 3882-3887
  • 35
    • 53349113909 scopus 로고    scopus 로고
    • The spectroscopic and structural data of 3 are given in the Supporting Information. CCDC 676473 (3), CCDC 676474 (8a), and CCDC 676475 (6) 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.
    • The spectroscopic and structural data of 3 are given in the Supporting Information. CCDC 676473 (3), CCDC 676474 (8a), and CCDC 676475 (6) 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.
  • 39
    • 0007351457 scopus 로고    scopus 로고
    • Tetraaryl butatrienes and hexapentaenes readily form dianion species: a J. M. Edinger, S. F. Sisenwines, A. R. Day, J. Org. Chem. 1971, 36, 3614-3619;
    • Tetraaryl butatrienes and hexapentaenes readily form dianion species: a) J. M. Edinger, S. F. Sisenwines, A. R. Day, J. Org. Chem. 1971, 36, 3614-3619;
  • 42
    • 53349125307 scopus 로고    scopus 로고
    • Rosenthal et al. attempted the hydrogenation of 1-zirconacyclopent-3-yne but identified no products (ref. [5b]); see also: a) M. A. Bach, thesis, Universität Rostock, 2007;
    • Rosenthal et al. attempted the hydrogenation of 1-zirconacyclopent-3-yne but identified no products (ref. [5b]); see also: a) M. A. Bach, thesis, Universität Rostock, 2007;
  • 44
    • 53349133500 scopus 로고    scopus 로고
    • The structural data for 6 are given in the Supporting Information; see ref. [9].
    • The structural data for 6 are given in the Supporting Information; see ref. [9].
  • 55
    • 0038333329 scopus 로고    scopus 로고
    • and references therein
    • Angew. Chem. Int. Ed. 2003, 42, 1794-1798, and references therein.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 1794-1798
  • 58
    • 53349130369 scopus 로고    scopus 로고
    • A report on 1-hafnacyclopenta-2,3-diene complexes appeared during the review process of this article: J. Ugolotti, G. Dierker, G. Kehr, R. Fröhlich, S. Grimme, G. Erker, Angew. Chem. 2008, 120, 2662-2665;
    • A report on "1-hafnacyclopenta-2,3-diene" complexes appeared during the review process of this article: J. Ugolotti, G. Dierker, G. Kehr, R. Fröhlich, S. Grimme, G. Erker, Angew. Chem. 2008, 120, 2662-2665;
  • 59
    • 53349116076 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 2622-2625.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 2622-2625
  • 69
    • 53349157926 scopus 로고    scopus 로고
    • Ring-flip inversion was observed for a 1-hafnacyclopenta-2,3- diene complex in ref, 21
    • Ring-flip inversion was observed for a "1-hafnacyclopenta-2,3- diene" complex in ref. [21].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.