메뉴 건너뛰기




Volumn 68, Issue 22, 2003, Pages 8726-8729

Mild Electrophilic Trifluoromethylation of β-Ketoesters and Silyl Enol Ethers with 5-Trifluoro Methyldibenzothiophenium Tetrafluoroborate

Author keywords

[No Author keywords available]

Indexed keywords

PHASE-TRANSFER CATALYSTS;

EID: 0142196823     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo034881e     Document Type: Article
Times cited : (86)

References (52)
  • 1
    • 0003536898 scopus 로고
    • Banks, R. E., Smart, B. E., Tatlow, J. C., Eds.; Plenum Press: New York
    • For general applications of organofluorine compounds: Organofluorine Chemistry: Principles and Commercial Applications; Banks, R. E., Smart, B. E., Tatlow, J. C., Eds.; Plenum Press: New York, 1994.
    • (1994) Organofluorine Chemistry: Principles and Commercial Applications
  • 2
    • 0142205642 scopus 로고    scopus 로고
    • Ojima, I., McCarthy, J. R., Welch, J. T., Eds.; ACS Symposium Series 639; American Chemical Society: Washington, DC
    • For the use of organofluorine compounds in medicinal and agrochemical science: (a) Biomedical Frontiers of Fluorine Chemistry; Ojima, I., McCarthy, J. R., Welch, J. T., Eds.; ACS Symposium Series 639; American Chemical Society: Washington, DC, 1996.
    • (1996) Biomedical Frontiers of Fluorine Chemistry
  • 6
    • 0142143662 scopus 로고    scopus 로고
    • Ramachandran, P. V., Eds.; ACS Symposium Series 746; American Chemical Society: Washington, DC; Chapters 16-18
    • For the use of organofluorine compounds in material chemistry: Asymmetric Fluoroorganic Chemistry; Synthesis, Applications, and Future Directions; Ramachandran, P. V., Eds.; ACS Symposium Series 746; American Chemical Society: Washington, DC, 2000; Chapters 16-18.
    • (2000) Asymmetric Fluoroorganic Chemistry; Synthesis, Applications, and Future Directions
  • 24
    • 0031140114 scopus 로고    scopus 로고
    • Recent articles on nucleophilic process: (a) Prakash, G. K. S.; Yudin, A. K. Chem. Rev. 1997, 97, 757-786.
    • (1997) Chem. Rev. , vol.97 , pp. 757-786
    • Prakash, G.K.S.1    Yudin, A.K.2
  • 38
    • 0000299945 scopus 로고    scopus 로고
    • (d) Umemoto, T. Chem. Rev. 1996, 96, 1757-1777.
    • (1996) Chem. Rev. , vol.96 , pp. 1757-1777
    • Umemoto, T.1
  • 46
    • 0037148980 scopus 로고    scopus 로고
    • For analogous electrophilic fluorination: Kim, D. Y.; Park, E. J. Org. Lett. 2002, 4, 545-547.
    • (2002) J. Org. Lett. , vol.4 , pp. 545-547
    • Kim, D.Y.1    Park, E.2
  • 47
    • 0142174489 scopus 로고    scopus 로고
    • note
    • Anhydrous and standard DMF give equal yields of trifluoromethylation.
  • 48
    • 0003592858 scopus 로고
    • The Organic Chemistry Monograph Series; W. A. Benjamin: Menlo Park, CA
    • House, H. O. Modern Synthetic Reactions, 2nd ed.; The Organic Chemistry Monograph Series; W. A. Benjamin: Menlo Park, CA, 1972; pp 492-628.
    • (1972) Modern Synthetic Reactions, 2nd Ed. , pp. 492-628
    • House, H.O.1
  • 50
    • 0142205641 scopus 로고    scopus 로고
    • note
    • Lithium enolate of 2-methyl-1-indanone treated with 2a gave 2-methyl-2-trifluoromethyl-1-indanone in 51% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.