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Volumn 50, Issue 31, 2011, Pages 7162-7166

A simple and highly efficient iron catalyst for a [2+2+2] cycloaddition to form pyridines

Author keywords

cycloaddition; heterocycles; iron; nitriles; pyridines

Indexed keywords

[2+2+2] CYCLOADDITION; DIPHOSPHINE LIGAND; HETEROCYCLES; HIGH REACTIVITY; IN-SITU; IRON CATALYST; IRON SALTS; NITRILES; ROOM TEMPERATURE;

EID: 79960638576     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201102001     Document Type: Article
Times cited : (164)

References (82)
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    • during proof correction of this manuscript, an iron-catalyzed [2+2+2] cycloaddition of an alkyne nitrile and an alkyne was reported; see:, B. R. D'Souza, T. K. Lane, J. Louie, Org. Lett. 2011, 13, 2936.
    • (2011) Org. Lett. , vol.13 , pp. 2936
    • D'Souza, B.R.1    Lane, T.K.2    Louie, J.3
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    • Only benzene-type products were formed in good to excellent yields, for details please see:, Y. Liu, X. Yan, N. Yang, C. Xi, Catal. Commun. 2011, 12, 489.
    • (2011) Catal. Commun. , vol.12 , pp. 489
    • Liu, Y.1    Yan, X.2    Yang, N.3    Xi, C.4
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    • A ferracyclopentadiene intermediate was previously isolated and characterized:, U. Zenneck, Angew. Chem. 1990, 102, 171
    • (1990) Angew. Chem. , vol.102 , pp. 171
    • Zenneck, U.1
  • 82
    • 3342989847 scopus 로고    scopus 로고
    • The large size difference between the terminal substituents plays a crucial role in the regioselectivity of these cycloaddition reactions; for details please see Ref. [5 m] and, T. N. Tekavec, A. M. Arif, J. Louie, Tetrahedron 2004, 60, 7431.
    • (2004) Tetrahedron , vol.60 , pp. 7431
    • Tekavec, T.N.1    Arif, A.M.2    Louie, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.