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Volumn , Issue 2, 2006, Pages 267-270

Tri-tert-butylphosphine is an efficient promoter for the trifluoromethylation reactions of aldehydes, ketones, imides and imines

Author keywords

Aldehydes; Fluorine; Imines; Lewis bases; Trifluoromethylation

Indexed keywords

ALDEHYDE DERIVATIVE; CARBONYL DERIVATIVE; FLUORINE DERIVATIVE; IMIDE; IMINE; KETONE DERIVATIVE; PHOSPHINE DERIVATIVE; REAGENT; SILICON DERIVATIVE;

EID: 32344446963     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-926223     Document Type: Article
Times cited : (58)

References (48)
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    • Prakash, G.K.S.1    Hu, J.2
  • 2
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    • Olah, G. A.; Chambers, R. D.; Prakash, G. K. S., Eds.; John Wiley and Sons: New York, Chap. 11, and references therein
    • (b) Farnham, W. B. In Synthetic Fluorine Chemistry; Olah, G. A.; Chambers, R. D.; Prakash, G. K. S., Eds.; John Wiley and Sons: New York, 1992, Chap. 11, and references therein.
    • (1992) Synthetic Fluorine Chemistry
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  • 24
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    • (b) Mukaiyama's method utilizing less basic LiOAc as a catalyst might be suitable for even base labile substrates. See: Mukaiyama, T.; Kawano, Y.; Fujisawa, H. Chem. Lett. 2005, 34, 88.
    • (2005) Chem. Lett. , vol.34 , pp. 88
    • Mukaiyama, T.1    Kawano, Y.2    Fujisawa, H.3
  • 34
    • 32344439526 scopus 로고    scopus 로고
    • Jpn. Kokai Tokkyo Koho JP 07118188A2
    • 3 has appeared in a patent. See: Fuchikami, T.; Hagiwara, T. Jpn. Kokai Tokkyo Koho JP 07118188A2;
    • Fuchikami, T.1    Hagiwara, T.2
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    • note
    • 3 (57 μL, 0.38 mmol) was added at r.t. The mixture was stirred at r.t. for 0.5 h; the reaction was concentrated under reduced pressure. The residue was chromatographed on silica gel using hexane to afford 2b in 99% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.