메뉴 건너뛰기




Volumn 15, Issue 35, 2009, Pages 8800-8806

Single and consecutive cyclization reactions of alkynyl carbene complexes and 8-azaheptafulvenes: direct access to poh cyclic pyrrole and indole derivatives

Author keywords

Carbenes; Chromium; Cyclization; Heterocycles; Indole; Pyrrole

Indexed keywords

ALKYNYLS; CARBENE COMPLEXES; CARBENES; CYCLIZATION REACTIONS; CYCLOPENTANNULATION; DEGREE OF SUBSTITUTION; DIELS-ALDER REACTION; DIENOPHILES; DIRECT ACCESS; FISCHER CARBENE COMPLEX; FUNCTIONALIZATIONS; HETEROCYCLES; HETEROCYCLIZATIONS; INDOLE; INDOLE DERIVATIVES; METAL CARBENES; ONE POT; PYRROLE; REGIO-SELECTIVE; RING CLOSURES; STRUCTURAL COMPLEXITY;

EID: 69749099906     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200901257     Document Type: Article
Times cited : (27)

References (74)
  • 1
    • 0000134377 scopus 로고
    • (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson), Pergamen, New York
    • Recent reviews: a) W. D. Wulff in Comprehensive Organometallic Chemistry II, Vol.12 (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson), Pergamen, New York, 1995, pp. 469-547;
    • (1995) Comprehensive Organometallic Chemistry II, Vol. , vol.12 , pp. 469-547
    • Wulff, W.D.1
  • 6
    • 0034301372 scopus 로고    scopus 로고
    • f)M. A. Sierra, Chem. Rev. 2000, 100, 3591-3637;
    • (2000) Chem. Rev. , vol.100 , pp. 3591-3637
    • Sierra, M.A.1
  • 8
    • 0000036185 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 3964-4002;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3964-4002
  • 24
    • 0034605941 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 4346-4348.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 4346-4348
  • 36
    • 40949151741 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 2459-2462;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 2459-2462
  • 39
    • 24944519327 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 5875-5878; [6+3]:
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 5875-5878
  • 44
    • 8444246793 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 5510-5513.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5510-5513
  • 48
    • 0041305921 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 3008-3011;
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 3008-3011
  • 56
    • 23744463209 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4981-4983.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4981-4983
  • 60
    • 0011731459 scopus 로고
    • The [8+2] cycloaddition between a 8-azaheptafulvene and dimethyl acetylendicarboxylate at 50°C was reported, see: K. Sanechika, S. Kajigaeshi, S. Kanemasa, Chem. Lett. 1977, 861-864.
    • (1977) Chem. Lett. , pp. 861-864
    • Sanechika, K.1    Kajigaeshi, S.2    Kanemasa, S.3
  • 61
    • 69749113096 scopus 로고    scopus 로고
    • 13CNMR spectroscopy, HRMS).
    • 13CNMR spectroscopy, HRMS).
  • 63
    • 69749101653 scopus 로고    scopus 로고
    • For a recent contribution from our group, see reference [13b]
    • For a recent contribution from our group, see reference [13b],
  • 64
    • 69749111169 scopus 로고    scopus 로고
    • CCDC-731620 (8) and 731619 (15) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC-731620 (8) and 731619 (15) 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.
  • 70
    • 69749116070 scopus 로고    scopus 로고
    • The indole framework is present in a huge number of bioactive compounds and natural products, mainly alkaloids: R. J. Sundberg in
    • The indole framework is present in a huge number of bioactive compounds and natural products, mainly alkaloids: R. J. Sundberg in Indoles, Academic Press, London, 1996.
    • (1996) Indoles, Academic Press, London
  • 71
    • 0034615797 scopus 로고    scopus 로고
    • For a review on indole synthesis, see
    • For a review on indole synthesis, see: G. W. Gribble, J. Chem. Soc. Perkin Trans 1 2000, 1045.
    • (2000) J. Chem. Soc. Perkin Trans , vol.1 , pp. 1045
    • Gribble, G.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.