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Volumn 2, Issue 1, 2013, Pages 50-53

Lewis-acid-catalyzed intramolecular aza-friedel-crafts reaction of N-tert-butanesulfinyl imines: Efficient synthesis of optically active 9-aminofluorene derivatives

Author keywords

9 aminofluorenes; Asymmetric synthesis; Aza Friedel Crafts reaction; Lewis acids; N tert butanesulfinyl imines

Indexed keywords


EID: 84896282957     PISSN: 21935807     EISSN: 21935807     Source Type: Journal    
DOI: 10.1002/ajoc.201200161     Document Type: Article
Times cited : (13)

References (56)
  • 48
    • 84899712490 scopus 로고    scopus 로고
    • See the Supporting Information for details.
    • See the Supporting Information for details.
  • 49
    • 84899749018 scopus 로고    scopus 로고
    • The direct use of TfOH as catalyst was examined. The reaction can be promoted in the presence of 10mol% of TfOH at room temperature; however, the yield (69%) and diastereoselectivity (84.5:15.5 d.r.) were not ideal.
    • The direct use of TfOH as catalyst was examined. The reaction can be promoted in the presence of 10mol% of TfOH at room temperature; however, the yield (69%) and diastereoselectivity (84.5:15.5 d.r.) were not ideal.
  • 50
    • 84899764259 scopus 로고    scopus 로고
    • (int)=0.0166). CCDC910838 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • (int)=0.0166). CCDC910838 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.
  • 51
    • 84899765180 scopus 로고    scopus 로고
    • For related crystal structures and theoretical calculations, see:
    • For related crystal structures and theoretical calculations, see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.