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Volumn 73, Issue 19, 2008, Pages 7451-7456

Auto-tandem catalysis in the synthesis of substituted quinolines from aldimines and electron-rich olefins: Cascade Povarov-hydrogen-transfer reaction

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; CHEMICAL REACTIONS; HYDROGEN; NITROGEN COMPOUNDS; NONMETALS; OLEFINS;

EID: 53049106528     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8009243     Document Type: Article
Times cited : (116)

References (37)
  • 11
    • 0030602266 scopus 로고    scopus 로고
    • For a review of tetrahydroquinoline synthesis, see
    • For a review of tetrahydroquinoline synthesis, see: Katritzky, A. R.; Rachwal, S.; Rachwal, B. Tetrahedron 1996, 52, 15031-15070.
    • (1996) Tetrahedron , vol.52 , pp. 15031-15070
    • Katritzky, A.R.1    Rachwal, S.2    Rachwal, B.3
  • 13
    • 9744257740 scopus 로고    scopus 로고
    • Definition of auto-tandem catalysis: Fogg, D. E.; dos Santos, E. N. Coord. Chem. Rev. 2004, 248, 2365-2379.
    • Definition of "auto-tandem catalysis": Fogg, D. E.; dos Santos, E. N. Coord. Chem. Rev. 2004, 248, 2365-2379.
  • 15
    • 0344924960 scopus 로고    scopus 로고
    • For recent representative examples for auto-tandem catalysis, see: a
    • For recent representative examples for auto-tandem catalysis, see: (a) Field, L. D.; Messerle, B. A.; Wren, S. L. Organometallics 2003, 22, 4393-4395.
    • (2003) Organometallics , vol.22 , pp. 4393-4395
    • Field, L.D.1    Messerle, B.A.2    Wren, S.L.3
  • 23
    • 34249906469 scopus 로고    scopus 로고
    • A part of this work was published as a preliminary communication: Shindoh, N.; Tokuyama, H.; Takasu, K. Tetrahedron Lett. 2007, 48, 4749-4753.
    • A part of this work was published as a preliminary communication: Shindoh, N.; Tokuyama, H.; Takasu, K. Tetrahedron Lett. 2007, 48, 4749-4753.
  • 25
    • 53049085003 scopus 로고    scopus 로고
    • After publication of our preliminary communication (ref 12), Mahajan and his co-workers reported an interesting synthetic study using Povarov-hydrogen-transfer reaction in the presence of Lewis acids; see: Bhargave, G.; Mohan, C.; Mahajan, M. P. Tetrahedron 2008, 64, 3017-3024.
    • After publication of our preliminary communication (ref 12), Mahajan and his co-workers reported an interesting synthetic study using Povarov-hydrogen-transfer reaction in the presence of Lewis acids; see: Bhargave, G.; Mohan, C.; Mahajan, M. P. Tetrahedron 2008, 64, 3017-3024.
  • 26
    • 0001741761 scopus 로고    scopus 로고
    • Hydrogen-transfer between 1,2-dihydroquinolines and imines has been reported by several groups; see: (a) Leardini, R.; Nanni, D.; Tundo, A.; Zanardi, G.; Ruggieri, F. J. Org. Chem. 1992, 57, 1842-1848.
    • Hydrogen-transfer between 1,2-dihydroquinolines and imines has been reported by several groups; see: (a) Leardini, R.; Nanni, D.; Tundo, A.; Zanardi, G.; Ruggieri, F. J. Org. Chem. 1992, 57, 1842-1848.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.