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Volumn 62, Issue 5, 2006, Pages 968-976

Synthesis of atropoisomeric pyridines via cobalt-catalyzed cocyclotrimerization of diynes with benzonitrile

Author keywords

Catalysis; Cobalt; Cocyclotrimerization; Organocatalysis; Pyridine

Indexed keywords

BENZONITRILE; COBALT; OXIDE; PYRIDINE DERIVATIVE;

EID: 29144437862     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.10.034     Document Type: Article
Times cited : (37)

References (85)
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  • 20
    • 0000814758 scopus 로고
    • [2+2+2] Cycloadditions
    • B.M. Trost I. Fleming L.A. Paquette Pergamon Oxford
    • N.E. Shore B.M. Trost I. Fleming L.A. Paquette [2+2+2] Cycloadditions Comprehensive Synthesis Vol. 5 1991 Pergamon Oxford 1129 1162
    • (1991) Comprehensive Synthesis , vol.5 , pp. 1129-1162
    • Shore, N.E.1
  • 21
    • 0000134376 scopus 로고
    • Transition Metal Alkyne Complexes: Transition Metal-Catalyzed Cyclotrimerization
    • E.W. Abel F.G.A. Stone G. Wilkinson L.S. Hegedus Pergamon Oxford
    • D.B. Grotjahn E.W. Abel F.G.A. Stone G. Wilkinson L.S. Hegedus Transition Metal Alkyne Complexes: Transition Metal-Catalyzed Cyclotrimerization Comprehensive Organometallic Chemistry II Vol. 12 1995 Pergamon Oxford 741
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 741
    • Grotjahn, D.B.1
  • 22
    • 0001119976 scopus 로고    scopus 로고
    • Cyclomerization of Alkynes
    • M. Beller C. Bolm Wiley Weinheim, Germany
    • H. Bönnemann, and W. Brijoux M. Beller C. Bolm Cyclomerization of Alkynes Transition Metals for Organic Synthesis Vol. 1 1998 Wiley Weinheim, Germany 114 135
    • (1998) Transition Metals for Organic Synthesis , vol.1 , pp. 114-135
    • Bönnemann, H.1    Brijoux, W.2
  • 66
    • 0022397082 scopus 로고
    • For reaction of α,β-diynes with nitriles in natural product synthesis, see: (a) C.A. Parnell, and K.P.C. Vollhardt Tetrahedron 41 1985 5791 5796
    • (1985) Tetrahedron , vol.41 , pp. 5791-5796
    • Parnell, C.A.1    Vollhardt, K.P.C.2
  • 77
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    • note
    • Jonas catalyst is very reactive and promotes cocyclotrimerization of alkynes with nitriles already at 20°C. (a) See Ref. 28a.
  • 81
    • 29144534970 scopus 로고    scopus 로고
    • (e) See Ref. 18
    • (e) See Ref. 18


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.