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Volumn 70, Issue 17, 2014, Pages 2816-2821

Asymmetric aldol reaction using a very simple primary amine catalyst: Divergent stereoselectivity by using 2,6-difluorophenyl moiety

Author keywords

Aldol reaction; Asymmetric catalysis; Isatin; Organocatalysis; Valine

Indexed keywords

ACETONE; ALDEHYDE DERIVATIVE; ALIPHATIC KETONE; AMINE; CYCLOALKANONE; ISATIN; ISATIN DERIVATIVE;

EID: 84897459975     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2014.02.059     Document Type: Article
Times cited : (14)

References (52)
  • 22
    • 11844259698 scopus 로고    scopus 로고
    • Wiley-VCH Weinheim, Germany
    • R. Mahrwald Modern Aldol Reactions Vols. 1 and 2 2004 Wiley-VCH Weinheim, Germany
    • (2004) Modern Aldol Reactions , vol.12 VOLS. AND
    • Mahrwald, R.1
  • 23
    • 60849085172 scopus 로고    scopus 로고
    • The single-crystal X-ray analysis of perfluorophenyl-N-prolinamide has been reported, where the stereoselectivity of aldol product was attributed to the enhanced NH acidity and conformation of the perfluorophenyl ring. For details, see
    • The single-crystal X-ray analysis of perfluorophenyl-N-prolinamide has been reported, where the stereoselectivity of aldol product was attributed to the enhanced NH acidity and conformation of the perfluorophenyl ring. For details, see: J.N. Moorthy, and S. Saha Eur. J. Org. Chem. 2009 739
    • (2009) Eur. J. Org. Chem. , pp. 739
    • Moorthy, J.N.1    Saha, S.2
  • 52
    • 84897427788 scopus 로고    scopus 로고
    • CCDC 978573 contains the supplementary of 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.