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Search for "redox chemistry" in Full Text gives 28 result(s) in Beilstein Journal of Organic Chemistry.

When gold can do what iodine cannot do: A critical comparison

  • Sara Hummel and
  • Stefan F. Kirsch

Beilstein J. Org. Chem. 2011, 7, 847–859, doi:10.3762/bjoc.7.97

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  • led to numerous elegant contributions in both heterocycle and carbocycle syntheses [14][15][16][17][18][19][20]. In general, these processes are easy to perform under simple reaction conditions: Significant redox chemistry is not involved. Since gold complexes show outstanding functional group
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Published 22 Jun 2011

Structure and reactivity in neutral organic electron donors derived from 4-dimethylaminopyridine

  • Jean Garnier,
  • Alan R. Kennedy,
  • Leonard E. A. Berlouis,
  • Andrew T. Turner and
  • John A. Murphy

Beilstein J. Org. Chem. 2010, 6, No. 73, doi:10.3762/bjoc.6.73

Graphical Abstract
  • the disalts. All of the cyclic voltammograms showed reversible redox chemistry, featuring the transfer of two electrons, as indicated by calibration with ferrocene/ferrocenium (Fc/Fc+). Restricting the bridge length to two carbons made donor 14 a less effective reducing agent (Figure 3) compared to 8
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Published 05 Jul 2010

Synthesis and redox behavior of new ferrocene- π-extended- dithiafulvalenes: An approach for anticipated organic conductors

  • Abdelwareth A. O. Sarhan,
  • Omar F. Mohammed and
  • Taeko Izumi

Beilstein J. Org. Chem. 2009, 5, No. 6, doi:10.3762/bjoc.5.6

Graphical Abstract
  • multicomponent electron donor systems by the Wittig–Horner reaction of the respective phosphonate ester 6 with different ferreocenylketones using the modifications introduced onto the reaction. The redox chemistry of the ferreocenylketones and these new π-conjugated hybrids 8, 10 and 11 has been studied using
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Published 19 Feb 2009
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