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Search for "Ullman coupling" in Full Text gives 3 result(s) in Beilstein Journal of Organic Chemistry.

The biomimetic synthesis of balsaminone A and ellagic acid via oxidative dimerization

  • Sharna-kay Daley and
  • Nadale Downer-Riley

Beilstein J. Org. Chem. 2020, 16, 2026–2031, doi:10.3762/bjoc.16.169

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  • Ullman coupling, Suzuki–Miyaura coupling and Stille coupling have dominated the field for the synthesis of biaryls [1][4]. Throughout the years, the exploration of oxidative dimerization reactions of electron-rich aromatic compounds, such as thiophenes, anilines and alkoxyarenes, in an attempt to
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Published 18 Aug 2020

Advances in the synthesis of functionalised pyrrolotetrathiafulvalenes

  • Luke J. O’Driscoll,
  • Sissel S. Andersen,
  • Marta V. Solano,
  • Dan Bendixen,
  • Morten Jensen,
  • Troels Duedal,
  • Jess Lycoops,
  • Cornelia van der Pol,
  • Rebecca E. Sørensen,
  • Karina R. Larsen,
  • Kenneth Myntman,
  • Christian Henriksen,
  • Stinne W. Hansen and
  • Jan O. Jeppesen

Beilstein J. Org. Chem. 2015, 11, 1112–1122, doi:10.3762/bjoc.11.125

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  • to the N-arylation of MPTTFs and BPTTFs using a variety of aryl halides. Keywords: heterocycles; protecting groups; sulfur chemistry; tetrathiafulvalene; Ullman coupling; Introduction Tetrathiafulvalene (TTF) derivatives are of considerable interest in the fields of supramolecular chemistry and
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Published 03 Jul 2015

A convenient method for preparing rigid-core ionic liquid crystals

  • Julien Fouchet,
  • Laurent Douce,
  • Benoît Heinrich,
  • Richard Welter and
  • Alain Louati

Beilstein J. Org. Chem. 2009, 5, No. 51, doi:10.3762/bjoc.5.51

Graphical Abstract
  • liquid crystalline phases and easily be doped by a large diversity of anions [11][12][13][14][15][16][17][18][19][20][21]. Variation of the N-substituents by Ullman coupling to extend the aromatic part is a facile means of creating this range [22][23]. Herein, we wish to report a solvent-free, N
  • species. Note that the peak at −0.8 V is probably due to the reduction of O2 which is difficult to eliminate from the solution. Conclusion In conclusion, we report synthetic methodology based on Ullman coupling to extend the imidazolium aromatic core. From this coupling product we have synthesized and
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Published 07 Oct 2009
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