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Search for "Suzuki cross-coupling" in Full Text gives 53 result(s) in Beilstein Journal of Organic Chemistry.

Graphical Abstract
  • inhibition nor any significant slowing of the photoreaction of the ligand was observed. Conclusion We have developed the synthesis of two highly fatigue resistant bis(terpyridinyl) diarylethenes by Suzuki cross coupling methods. The photochemical behavior of the free ligand 10a met our expectations regarding
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Published 26 May 2010

Efficient and improved synthesis of Telmisartan

  • A. Sanjeev Kumar,
  • Samir Ghosh and
  • G. N. Mehta

Beilstein J. Org. Chem. 2010, 6, No. 25, doi:10.3762/bjoc.6.25

Graphical Abstract
  • antihypertensive drug Telmisartan has been developed, featuring a Suzuki cross-coupling for the construction of the biaryl moiety and a regiospecific reductive amination-condensation sequence for the synthesis of the central benzimidazole. Experimental All solvents and reagents were purchased from the commercial
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Published 11 Mar 2010

A convenient catalyst system for microwave accelerated cross- coupling of a range of aryl boronic acids with aryl chlorides

  • Matthew L. Clarke,
  • Marcia B. France,
  • Jose A. Fuentes,
  • Edward J. Milton and
  • Geoffrey J. Roff

Beilstein J. Org. Chem. 2007, 3, No. 18, doi:10.1186/1860-5397-3-18

Graphical Abstract
  • microwave accelerated cross-coupling procedure between aryl chlorides with a range of boronic acids has been developed. An explanation for the low reactivity of highly fluorinated boronic acids in Suzuki coupling is provided. Background The Suzuki cross-coupling represents an extremely useful method for
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Preliminary Communication
Published 30 May 2007
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