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Volumn 13, Issue 5, 2011, Pages 832-835

Highly enantioselective synthesis of polysubstituted tetrahydroquinolines via organocatalytic Michael/Aza-Henry tandem reactions

Author keywords

[No Author keywords available]

Indexed keywords

1,2,3,4 TETRAHYDROQUINOLINE; 1,2,3,4-TETRAHYDROQUINOLINE; QUINOLINE DERIVATIVE; THIOUREA;

EID: 79952147389     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol103069d     Document Type: Article
Times cited : (93)

References (57)
  • 30
    • 48849094479 scopus 로고    scopus 로고
    • For reviews on organocatalytic reactions, see
    • For reviews on organocatalytic reactions, see: Dondoni, A.; Massi, A. Angew. Chem., Int. Ed. 2008, 47, 4638
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 4638
    • Dondoni, A.1    Massi, A.2
  • 34
    • 34250613134 scopus 로고    scopus 로고
    • For organocatalyst-mediated cross Michael reactions
    • For organocatalyst-mediated cross Michael reactions, see: Tsogoeva, S. B. Eur. J. Org. Chem. 2007, 1701
    • (2007) Eur. J. Org. Chem. , pp. 1701
    • Tsogoeva, S.B.1
  • 45
    • 30444443444 scopus 로고    scopus 로고
    • For recent reviews of tandem reactions, see
    • For recent reviews of tandem reactions, see: Guo, H.-C.; Ma, J.-A. Angew. Chem., Int. Ed. 2006, 45, 354
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 354
    • Guo, H.-C.1    Ma, J.-A.2
  • 55
    • 79952157704 scopus 로고    scopus 로고
    • CCDC 787334 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 787334 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.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.