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Search for "Suzuki cross-coupling" in Full Text gives 52 result(s) in Beilstein Journal of Organic Chemistry.

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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Full Research Paper
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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Supp Info
Preliminary Communication
Published 30 May 2007
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