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Reaction of 5-Allyl-2,3,5-trichloro-4,4-dimethoxycyclopent-2-en-1-one with amino acids

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Abstract

5-Allyl-2,3,5-trichloro-4,4-dimethoxycyclopent-2-en-1-one reacts with L-proline and L-methionine methyl esters to give diastereoisomeric mixtures of the corresponding chlorine replacement products at C3.

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Authors and Affiliations

  1. Institute of Organic Chemistry, Ufa Research Center, Russian Academy of Sciences, pr. Oktyabrya 71, Ufa, 450054, Bashkortostan, Russia

    F. A. Gimalova, V. A. Egorov, S. A. Torosyan & M. S. Miftakhov

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  1. F. A. Gimalova
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  2. V. A. Egorov
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  3. S. A. Torosyan
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  4. M. S. Miftakhov
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Additional information

Original Russian Text © F.A. Gimalova, V.A. Egorov, S.A. Torosyan, M.S. Miftakhov, 2007, published in Zhurnal Organicheskoi Khimii, 2007, Vol. 43, No. 7, pp. 987–989.

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Gimalova, F.A., Egorov, V.A., Torosyan, S.A. et al. Reaction of 5-Allyl-2,3,5-trichloro-4,4-dimethoxycyclopent-2-en-1-one with amino acids. Russ J Org Chem 43, 981–983 (2007). https://doi.org/10.1134/S1070428007070068

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  • DOI: https://doi.org/10.1134/S1070428007070068

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