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Volumn 52, Issue 20, 2013, Pages 5319-5322

Amine-promoted asymmetric (4+2) annulations for the enantioselective synthesis of tetrahydropyridines: A traceless and recoverable auxiliary strategy

Author keywords

cycloaddition; dienamine; elimination; nucleophilic addition; tetrahydropyridine

Indexed keywords

DIENAMINE; ELIMINATION; ENANTIOSELECTIVE SYNTHESIS; IN-SITU REACTIONS; NUCLEOPHILIC ADDITIONS; SECONDARY AMINES; TETRAHYDROPYRIDINE; TETRAHYDROPYRIDINES;

EID: 84877294647     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201300526     Document Type: Article
Times cited : (46)

References (66)
  • 4
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    • in (Ed.: G. A. Cordell), Academic Press, San Diego
    • J. P. Michael, in The Alkaloids, Vol. 55 (Ed.:, G. A. Cordell,), Academic Press, San Diego, 2001
    • (2001) The Alkaloids, Vol. 55
    • Michael, J.P.1
  • 61
    • 77957120788 scopus 로고    scopus 로고
    • After conversion of 7 into 2-(4-(trifluoromethyl)phenyl)piperidine, the absolute configuration was determined by comparing the optical rotation with the literature value
    • After conversion of 7 into 2-(4-(trifluoromethyl)phenyl)piperidine, the absolute configuration was determined by comparing the optical rotation with the literature value:, J. E. D. Martins, M. A. C. Redondo, M. Wills, Tetrahedron: Asymmetry 2010, 21, 2258.
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 2258
    • Martins, J.E.D.1    Redondo, M.A.C.2    Wills, M.3
  • 66
    • 84877270103 scopus 로고    scopus 로고
    • CCDC 920167 (5 d) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 920167 (5 d) 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.