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1
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33744510833
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For an overview see:. Dyker G. (Ed), Wiley-VCH, Weinheim
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For an overview see:. In: Dyker G. (Ed). Handbook of C-H Transformations (2005), Wiley-VCH, Weinheim
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(2005)
Handbook of C-H Transformations
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2
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43849091700
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For recent reviews see:
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For recent reviews see:
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5
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43849094120
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For recent rare examples of biaryl formation using this methodology see:
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For recent rare examples of biaryl formation using this methodology see:
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7
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34547960227
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Dwight T.A., Rue N.R., Charyk D., Josselyn R., and DeBoef B. Org. Lett. 9 (2007) 3137
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(2007)
Org. Lett.
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Dwight, T.A.1
Rue, N.R.2
Charyk, D.3
Josselyn, R.4
DeBoef, B.5
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13
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0025189573
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See also:
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Bringmann G., Jansen J.R., Reuscher H., Ru{combining double acute accent}benacker M., Peters K., and von Schnering H.G. Tetrahedron Lett. 31 (1990) 643 See also:
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(1990)
Tetrahedron Lett.
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Bringmann, G.1
Jansen, J.R.2
Reuscher, H.3
Rubenacker, M.4
Peters, K.5
von Schnering, H.G.6
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15
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0034721428
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Bringmann G., Pabst T., Henschel P., Kraus J., Peters K., Peters E.-M., Rycroft D.S., and Connolly J.D. J. Am. Chem. Soc. 122 (2000) 9127
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(2000)
J. Am. Chem. Soc.
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Bringmann, G.1
Pabst, T.2
Henschel, P.3
Kraus, J.4
Peters, K.5
Peters, E.-M.6
Rycroft, D.S.7
Connolly, J.D.8
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17
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33645995754
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Hostyn S., Maes B.U.W., van Baelen G., Gulevskaya A., Meyers C., and Smits K. Tetrahedron 62 (2006) 4676
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(2006)
Tetrahedron
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, pp. 4676
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Hostyn, S.1
Maes, B.U.W.2
van Baelen, G.3
Gulevskaya, A.4
Meyers, C.5
Smits, K.6
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21
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0003607021
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Katritzky A.R., Rees C.W., and Scriven E.F. (Eds), Pergamon, Oxford
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In: Katritzky A.R., Rees C.W., and Scriven E.F. (Eds). Comprehensive Heterocyclic Chemistry II (1996), Pergamon, Oxford
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(1996)
Comprehensive Heterocyclic Chemistry II
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22
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0036826933
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For a review on the isolation and synthesis of biologically active carbazoles see:
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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
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(2002)
Chem. Rev.
, vol.102
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Knölker, H.-J.1
Reddy, K.R.2
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23
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0000906771
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For a discussion, see:
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For a discussion, see:. Grushin V.V., and Alper H. Chem. Rev. 94 (1994) 1047
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(1994)
Chem. Rev.
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, pp. 1047
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Grushin, V.V.1
Alper, H.2
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24
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43849093573
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For recent examples of the use of tethered aryl chloride substrates in the arylation reactions via C-H activation see:
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For recent examples of the use of tethered aryl chloride substrates in the arylation reactions via C-H activation see:
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31
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4944231418
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For an overview of biological effects of organofluorine chemistry, see the special issue on Fluorine in the Life Sciences
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For an overview of biological effects of organofluorine chemistry, see the special issue on Fluorine in the Life Sciences,. ChemBioChem 5 (2004) 557-726
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(2004)
ChemBioChem
, vol.5
, pp. 557-726
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32
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43849101509
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note
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Limited precedents exist for the formation of fluorinated carbazoles, see Ref. 16.
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33
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0035961019
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3 in a range of coupling reactions, see:
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3 in a range of coupling reactions, see:. Netherton M.R., and Fu G.C. Org. Lett. 3 (2001) 4295
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(2001)
Org. Lett.
, vol.3
, pp. 4295
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Netherton, M.R.1
Fu, G.C.2
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34
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43849093239
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note
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++H]=234.
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36
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43849100082
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note
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Despite repeated attempts, we were unable to obtain better microanalytical data.
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38
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43849096021
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Oxford Diffraction, Abingdon, UK
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SCALE3 ABSPACK (2007), Oxford Diffraction, Abingdon, UK
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(2007)
SCALE3 ABSPACK
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