A short and efficient synthesis of valsartan via a Negishi reaction

Samir Ghosh, A. Sanjeev Kumar and G. N. Mehta
Beilstein J. Org. Chem. 2010, 6, No. 27. https://doi.org/10.3762/bjoc.6.27

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A short and efficient synthesis of valsartan via a Negishi reaction
Samir Ghosh, A. Sanjeev Kumar and G. N. Mehta
Beilstein J. Org. Chem. 2010, 6, No. 27. https://doi.org/10.3762/bjoc.6.27

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Ghosh, S.; Kumar, A. S.; Mehta, G. N. Beilstein J. Org. Chem. 2010, 6, No. 27. doi:10.3762/bjoc.6.27

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  • Malik, M. A.; Wani, M. Y.; Al-Thabaiti, S. A.; Shiekh, R. A. Tetrazoles as carboxylic acid isosteres: chemistry and biology. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2013, 78, 15–37. doi:10.1007/s10847-013-0334-x
  • Colacino, E.; Martinez, J.; Lamaty, F. doi:10.1002/9781118342886.ch2

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  • BURGBACHER JENS; HAHN BJOERN THOMAS; RAMPF FLORIAN ANDREAS; SCHNEEBERGER RICARDO. HIGHLY CRYSTALLINE VALSARTAN. WO 2012016969 A1, Feb 9, 2012.
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