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Volumn 72, Issue 18, 2007, Pages 6905-6917

CF3 oxonium salts, O-(trifluoromethyl)dibenzofuranium salts: In situ synthesis, properties, and application as a real CF3+ species reagent

Author keywords

[No Author keywords available]

Indexed keywords

COUNTERANIONS; DIBENZOFURANIUM SALTS; NUCLEOPHILICITY; RING SUBSITITUENTS;

EID: 34548763017     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo070896r     Document Type: Article
Times cited : (196)

References (48)
  • 1
    • 34548748205 scopus 로고    scopus 로고
    • Fabulous Fluorine. Chem. Eng. News 2006, June 5, 15-32.
    • Fabulous Fluorine. Chem. Eng. News 2006, June 5, 15-32.
  • 2
    • 0003420735 scopus 로고
    • Filler, R, Kobayashi, Y, Eds, Kodansha Ltd, Tokyo, Japan
    • (a) Biomedical Aspects of Fluorine Chemistry; Filler, R., Kobayashi, Y., Eds.; Kodansha Ltd.: Tokyo, Japan, 1982.
    • (1982) Biomedical Aspects of Fluorine Chemistry
  • 3
    • 0003907264 scopus 로고
    • Welch, J. T, Eswarakrishman, S, Eds, A Wiley-Interscience Publication, John Wiley & Sons, Inc, New York
    • (b) Fluorine in Bioorganic Chemistry; Welch, J. T., Eswarakrishman, S., Eds.; A Wiley-Interscience Publication, John Wiley & Sons, Inc.: New York, 1991.
    • (1991) Fluorine in Bioorganic Chemistry
  • 6
    • 0003518240 scopus 로고    scopus 로고
    • Ojima, I, McCarthy, J. R, Welch, J. T, Eds, ACS Books; American Chemical Society: Washington, DC
    • (e) Biomedical Frontiers of Fluorine Chemistry; Ojima, I., McCarthy, J. R., Welch, J. T., Eds.; ACS Books; American Chemical Society: Washington, DC, 1996.
    • (1996) Biomedical Frontiers of Fluorine Chemistry
  • 9
    • 34250656871 scopus 로고    scopus 로고
    • Fluorine-Containing Synthons
    • Soloshonok, V. A, Ed, American Chemical Society: Washington, DC
    • (b) Fluorine-Containing Synthons; Soloshonok, V. A., Ed.; ACS Symp. Ser. No. 911; American Chemical Society: Washington, DC, 2005.
    • (2005) ACS Symp. Ser , vol.911
  • 25
    • 34548735423 scopus 로고    scopus 로고
    • It has been known that CF3+ is generated in a gas phase. See the following recent paper: Mayer, P. S, Leblanc, D, Morton, T. H. J. Am. Chem. Soc. 2002, 124, 12185-14194
    • + is generated in a gas phase. See the following recent paper: Mayer, P. S.; Leblanc, D.; Morton, T. H. J. Am. Chem. Soc. 2002, 124, 12185-14194.
  • 31
    • 34548759178 scopus 로고    scopus 로고
    • + or δ+.
    • + or δ+.
  • 47
    • 0030975660 scopus 로고    scopus 로고
    • 3 substituents of aromatic rings: Ferraris, D.; Cox, C.; Anand, R.; Lectka, T. J. Am. Chem. Soc. 1997, 119, 4319-4320.
    • 3 substituents of aromatic rings: Ferraris, D.; Cox, C.; Anand, R.; Lectka, T. J. Am. Chem. Soc. 1997, 119, 4319-4320.
  • 48
    • 0001590919 scopus 로고
    • Roe, A. Org. React. 1968, 4, 193-228.
    • (1968) Org. React , vol.4 , pp. 193-228
    • Roe, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.