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2-Bromo-3,4,4-trichlorobut-3-enoates of certain natural alcohols, phenols, and oximes of carbonyl compounds

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Chemistry of Natural Compounds Aims and scope

Abstract

Previously undescribed 2-bromo-3,4,4-trichlorobut-3-enoates 1b-23b were synthesized in 84–91% yield from natural alcohols including terpenes and steroids, plant phenols, and oximes of natural carbonyl compounds 1a-23a by reaction of 2-bromo-3,4,4-trichlorobut-3-enoyl chloride in the presence of pyridine.

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References

  1. B. Testa, S. D. Kramer, H. Wunderli-Allenspach, and G. Folkers, Pharmacokinetic Profiling in Drug Research. Biological, Physicochemical, and Computational Strategies, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany (2005).

    Google Scholar 

  2. New Medicinal Preparations: Successes and Promise [in Russian], Gilem, Ufa (2005).

  3. S. K. Petkevich, E. A. Dikusar, V. I. Potkin, R. V. Kaberdin, K. L. Moiseichuk, A. P. Yuvchenko, and P. V. Kurman, Zh. Obshch. Khim., 74, 642 (2004).

    Google Scholar 

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Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 212–215, May–June, 2006.

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Dikusar, E.A., Potkin, V.I., Kozlov, N.G. et al. 2-Bromo-3,4,4-trichlorobut-3-enoates of certain natural alcohols, phenols, and oximes of carbonyl compounds. Chem Nat Compd 42, 254–258 (2006). https://doi.org/10.1007/s10600-006-0093-7

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  • DOI: https://doi.org/10.1007/s10600-006-0093-7

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