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Volumn 2, Issue 14, 2000, Pages 2101-2103

New stable reagents for the nucleophilic trifluoromethylation. 1. Trifluoromethylation of carbonyl compounds with N-formylmorpholine derivatives

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EID: 0000102197     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol005987o     Document Type: Article
Times cited : (107)

References (14)
  • 2
    • 0003642839 scopus 로고    scopus 로고
    • Baasner, B., Hagemann, H., Tatlow, J. C., Eds; Houben-Weyl: Methods of Organic Chemistry; Thieme: Stuttgart
    • T. In Organo-Fluorine Compounds; Baasner, B., Hagemann, H., Tatlow, J. C., Eds; Houben-Weyl: Methods of Organic Chemistry; Thieme: Stuttgart, 1999; Vol. E10a, 18-26.
    • (1999) Organo-Fluorine Compounds , vol.E10A , pp. 18-26
    • Groß, U.1    Rüdiger, St.2
  • 5
    • 0003132813 scopus 로고
    • Chemistry of organic fluorine compounds II. A critical review
    • American Chemical Society: Washington, DC
    • (c) Hudlicky, M.; Pavlath, A. E. Chemistry of Organic Fluorine Compounds II. A critical Review; ACS Monograph 187; American Chemical Society: Washington, DC, 1995.
    • (1995) ACS Monograph , vol.187
    • Hudlicky, M.1    Pavlath, A.E.2
  • 14
    • 0041509320 scopus 로고    scopus 로고
    • note
    • Typical Procedure. To a solution of 3 (2 mmol) and the electrophile (1 mmol) in DME (1 mL) was added a catalytic amount (≈10% mol) of CsF (dried at 250°C and stored at 110°C). The mixture was heated at 80 °C for 5 h. Then, the crude mixture was directly purified by chromatography over silica gel.


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