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Volumn , Issue 9, 2005, Pages 1834-1848

Coupling-isomerization-enamine addition-cyclocondensation sequences: A multicomponent approach to substituted and annelated pyridines

Author keywords

Alkynes; Catalysis; Cross Couplings; Cyclocondensation; Pyridines

Indexed keywords


EID: 18744382742     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200400828     Document Type: Article
Times cited : (37)

References (56)
  • 6
    • 0037907937 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1253-1256.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1253-1256
  • 14
    • 85011588750 scopus 로고
    • (Eds.: H. Suschitzky, E. F. V. Scriven), Pergamon Press, Oxford
    • b) J. F. Toomey, R. Murugan, in Progress in Heterocyclic Chemistry (Eds.: H. Suschitzky, E. F. V. Scriven), Pergamon Press, Oxford, 1994, vol. 6, pp. 206.
    • (1994) Progress in Heterocyclic Chemistry , vol.6 , pp. 206
    • Toomey, J.F.1    Murugan, R.2
  • 15
    • 0028312466 scopus 로고
    • For reviews see, for example: a) A. O. Plunkett, Nat. Prod. Rep. 1994, 11, 581-590;
    • (1994) Nat. Prod. Rep. , vol.11 , pp. 581-590
    • Plunkett, A.O.1
  • 18
    • 0004228346 scopus 로고
    • (Ed.: A. Brossi), Academic Press, New York
    • d) A. Numata, T. Ibuka, in The Alkaloids (Ed.: A. Brossi), Academic Press, New York 1987, Vol. 31;
    • (1987) The Alkaloids , vol.31
    • Numata, A.1    Ibuka, T.2
  • 36
    • 0004231652 scopus 로고
    • VCH, Weinheim, New York Basel, chapter 5.2
    • For general syntheses of pyridines see, for example: a) T. L. Gilchrist, Heterocyclenchemie, VCH, Weinheim, New York Basel, 1995, chapter 5.2;
    • (1995) Heterocyclenchemie
    • Gilchrist, T.L.1
  • 41
    • 0347155091 scopus 로고    scopus 로고
    • For enamine additions to enones generated in situ from Mannich bases see, for example: a) D. Sielemann, R. Keuper, N. Risch, J. Prakt. Chem. 1999, 341, 487-491;
    • (1999) J. Prakt. Chem. , vol.341 , pp. 487-491
    • Sielemann, D.1    Keuper, R.2    Risch, N.3
  • 44
    • 18744414838 scopus 로고    scopus 로고
    • note
    • CCDC-255818 (for 4b), -255817 (for 4g), -256133 (for 6), - 256134 (for 11), -256135 (for 11i), -256136 (for 11o), -256137 (for 14b), and -256138 (for 14c) 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.
  • 49
    • 85012738894 scopus 로고
    • (Eds.: H. Suschitzky, E. F. V. Scriven), Pergamon Press, Oxford
    • c) D. L. Boger, M. Patel, in Progress in Heterocyclic Chemistry (Eds.: H. Suschitzky, E. F. V. Scriven), Pergamon Press, Oxford, 1989, vol. 1.
    • (1989) Progress in Heterocyclic Chemistry , vol.1
    • Boger, D.L.1    Patel, M.2
  • 50
    • 0004127279 scopus 로고    scopus 로고
    • Wavefunction Inc.: Irvine, CA
    • PC Spartan Pro, Wavefunction Inc.: Irvine, CA, 2002.
    • (2002) PC Spartan Pro
  • 51
    • 0004127279 scopus 로고    scopus 로고
    • Wavefunction Inc.: Irvine, CA
    • Solvation model SM 5.4 (Cramer, Truhlar), as implemented in PC Spartan Pro, Wavefunction Inc.: Irvine, CA, 2002.
    • (2002) PC Spartan Pro


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.