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Volumn 14, Issue 25, 2008, Pages 7508-7512

C-H insertion processes on stabilized indolyl and ortho-aminophenyl fischer carbene complexes: Synthesis of azepino[3,2,1-hi] indole, benzazepine and indole derivatives

Author keywords

Benzazepines; C H insertion; Carbenes; Cascades; Heterocycles

Indexed keywords

BENZAZEPINES; C-H INSERTION; CARBENES; CASCADES; HETEROCYCLES;

EID: 53849134521     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200801132     Document Type: Conference Paper
Times cited : (15)

References (65)
  • 3
    • 0000134377 scopus 로고
    • Eds, E. W. Abel, F. G. A. Stone, G. Wilkinson, Pergamon, New York
    • a) W. D. Wulff in Comprehensive Organometallic Chemistry II, Vol. 12 (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson), Pergamon, New York, 1995, pp. 469-547;
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 469-547
    • Wulff, W.D.1
  • 4
    • 0000951659 scopus 로고
    • Eds, E. W. Abel, F. G. A. Stone, G. Wilkinson, Pergamon, New York
    • b) L. S. Hegedus in Comprehensive Organometallic Chemistry 11, Vol. 12 (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson), Pergamon, New York, 1995, pp. 549;
    • (1995) Comprehensive Organometallic Chemistry 11 , vol.12 , pp. 549
    • Hegedus, L.S.1
  • 7
    • 0034301372 scopus 로고    scopus 로고
    • e) M. A. Sierra, Chem. Rev. 2000, 100, 3591-3638;
    • (2000) Chem. Rev , vol.100 , pp. 3591-3638
    • Sierra, M.A.1
  • 14
    • 0000036185 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 3964-4002;
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 3964-4002
  • 17
    • 0000633297 scopus 로고
    • Ed, G. Pattenden, Pergamon Press, Oxford
    • a) D. F. Taber in Comprehensive Organic Synthesis, Vol.3 (Ed.: G. Pattenden), Pergamon Press, Oxford, 1991, pp. 1045-1062;
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 1045-1062
    • Taber, D.F.1
  • 18
    • 0008442196 scopus 로고
    • Homogeneous Transition Metal Catalysts in Organic Synthesis
    • Eds, W. R. Moser, D. W. Slocum, American Chemical Society, Washington, DC, Chapter 30;
    • b) M. P. Doyle in Homogeneous Transition Metal Catalysts in Organic Synthesis; (Eds.: W. R. Moser, D. W. Slocum), ACS Advanced Chemistry Series 230, American Chemical Society, Washington, DC, 1992, Chapter 30;
    • (1992) ACS Advanced Chemistry Series , vol.230
    • Doyle, M.P.1
  • 34
    • 0034605941 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 4346-4348;
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 4346-4348
  • 41
    • 5744224426 scopus 로고    scopus 로고
    • Ed, G. A. Cordell, Academic Press, New York, Chapter 9;
    • c) J. E. Saxton, in The Alkaloids, Vol. 50 (Ed.: G. A. Cordell), Academic Press, New York, 1998, Chapter 9;
    • (1998) The Alkaloids , vol.50
    • Saxton, J.E.1
  • 42
    • 0347225187 scopus 로고    scopus 로고
    • Ed, G. A. Cordell, Academic Press, New York, Chapter 1;
    • d) J. E. Saxton, in The Alkaloids, Vol. 51 (Ed.: G. A. Cordell), Academic Press, New York, 1998, Chapter 1;
    • (1998) The Alkaloids , vol.51
    • Saxton, J.E.1
  • 44
    • 53849132995 scopus 로고    scopus 로고
    • K. C. Nicolaou, S. A. Snyder, Classics in Total Synthesis II, Wiley-VCH, Weinheim, 2003, Chapters 5, 8, 12, 18,19, 20 and 22, pp. 639.
    • f) K. C. Nicolaou, S. A. Snyder, Classics in Total Synthesis II, Wiley-VCH, Weinheim, 2003, Chapters 5, 8, 12, 18,19, 20 and 22, pp. 639.
  • 46
    • 0003260139 scopus 로고    scopus 로고
    • An example of the formation of a seven-membered ring by C-H insertion involving an intramolecular transannular radical cyclization has been reported: U. Willie, Org. Lett. 2000, 2, 3485-3488
    • An example of the formation of a seven-membered ring by C-H insertion involving an intramolecular transannular radical cyclization has been reported: U. Willie, Org. Lett. 2000, 2, 3485-3488.
  • 47
    • 53849107071 scopus 로고    scopus 로고
    • We have recently described a 1.5-hydride transfer/cyclization process of ortho-aminophenyl alkynyl Fischer carbene complexes: J. Barluenga, M. Fañanás-Mastral, F. Aznar, C. Valdês, Angew. Chem. 2008, 120, 6696-6699;
    • We have recently described a 1.5-hydride transfer/cyclization process of ortho-aminophenyl alkynyl Fischer carbene complexes: J. Barluenga, M. Fañanás-Mastral, F. Aznar, C. Valdês, Angew. Chem. 2008, 120, 6696-6699;
  • 48
    • 53249123367 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 6594-6597.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 6594-6597
  • 49
    • 53849108039 scopus 로고    scopus 로고
    • CCDC 690594 (6a-maj) contains 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 690594 (6a-maj) contains 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.
  • 53
    • 0042269875 scopus 로고
    • For representative examples of cyclopentannulation processes of Fischer carbene complexes, see: a
    • For representative examples of cyclopentannulation processes of Fischer carbene complexes, see: a) J. Barluenga, F. Aznar, S. Barluenga, J. Chem. Soc. Chem. Commun. 1995, 1973-1974;
    • (1995) J. Chem. Soc. Chem. Commun , pp. 1973-1974
    • Barluenga, J.1    Aznar, F.2    Barluenga, S.3
  • 57
    • 0037176253 scopus 로고    scopus 로고
    • For leading references of synthesis of 2-alkyl indoles from 2-haloanilines see: a
    • For leading references of synthesis of 2-alkyl indoles from 2-haloanilines see: a) J. L. Rutherford, M. P. Rainka, S. L. Buchwald, J. Am. Chem. Soc. 2002, 124, 15168-15169;
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 15168-15169
    • Rutherford, J.L.1    Rainka, M.P.2    Buchwald, S.L.3
  • 61
    • 34250373793 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 2284-2287;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 2284-2287


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.