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Volumn 64, Issue 26, 2008, Pages 6038-6050

Intramolecular direct arylation in the synthesis of fluorinated carbazoles

Author keywords

[No Author keywords available]

Indexed keywords

2 CHLOROANILINE; ANILINE DERIVATIVE; BROMIDE; CARBAZOLE DERIVATIVE;

EID: 43849106837     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.01.143     Document Type: Article
Times cited : (63)

References (40)
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    • For an overview see:. In: Dyker G. (Ed). Handbook of C-H Transformations (2005), Wiley-VCH, Weinheim
    • (2005) Handbook of C-H Transformations
  • 2
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    • For recent reviews see:
    • For recent reviews see:
  • 5
    • 43849094120 scopus 로고    scopus 로고
    • For recent rare examples of biaryl formation using this methodology see:
    • For recent rare examples of biaryl formation using this methodology see:
  • 21
    • 0003607021 scopus 로고    scopus 로고
    • Katritzky A.R., Rees C.W., and Scriven E.F. (Eds), Pergamon, Oxford
    • In: Katritzky A.R., Rees C.W., and Scriven E.F. (Eds). Comprehensive Heterocyclic Chemistry II (1996), Pergamon, Oxford
    • (1996) Comprehensive Heterocyclic Chemistry II
  • 22
    • 0036826933 scopus 로고    scopus 로고
    • For a review on the isolation and synthesis of biologically active carbazoles see:
    • For a review on the isolation and synthesis of biologically active carbazoles see:. Knölker H.-J., and Reddy K.R. Chem. Rev. 102 (2002) 4303
    • (2002) Chem. Rev. , vol.102 , pp. 4303
    • Knölker, H.-J.1    Reddy, K.R.2
  • 23
    • 0000906771 scopus 로고
    • For a discussion, see:
    • For a discussion, see:. Grushin V.V., and Alper H. Chem. Rev. 94 (1994) 1047
    • (1994) Chem. Rev. , vol.94 , pp. 1047
    • Grushin, V.V.1    Alper, H.2
  • 24
    • 43849093573 scopus 로고    scopus 로고
    • For recent examples of the use of tethered aryl chloride substrates in the arylation reactions via C-H activation see:
    • For recent examples of the use of tethered aryl chloride substrates in the arylation reactions via C-H activation see:
  • 31
    • 4944231418 scopus 로고    scopus 로고
    • For an overview of biological effects of organofluorine chemistry, see the special issue on Fluorine in the Life Sciences
    • For an overview of biological effects of organofluorine chemistry, see the special issue on Fluorine in the Life Sciences,. ChemBioChem 5 (2004) 557-726
    • (2004) ChemBioChem , vol.5 , pp. 557-726
  • 32
    • 43849101509 scopus 로고    scopus 로고
    • note
    • Limited precedents exist for the formation of fluorinated carbazoles, see Ref. 16.
  • 33
    • 0035961019 scopus 로고    scopus 로고
    • 3 in a range of coupling reactions, see:
    • 3 in a range of coupling reactions, see:. Netherton M.R., and Fu G.C. Org. Lett. 3 (2001) 4295
    • (2001) Org. Lett. , vol.3 , pp. 4295
    • Netherton, M.R.1    Fu, G.C.2
  • 34
    • 43849093239 scopus 로고    scopus 로고
    • note
    • ++H]=234.
  • 36
    • 43849100082 scopus 로고    scopus 로고
    • note
    • Despite repeated attempts, we were unable to obtain better microanalytical data.
  • 38
    • 43849096021 scopus 로고    scopus 로고
    • Oxford Diffraction, Abingdon, UK
    • SCALE3 ABSPACK (2007), Oxford Diffraction, Abingdon, UK
    • (2007) SCALE3 ABSPACK


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.