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Prostanoids: LXXIV. 2,3-Dichloro- 4,4-ethylenedioxy-2-cyclopentenone in the Synthesis of Analogs of Marine Prostanoid

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Abstract

Transformations of readily accessible 2,3-dichloro-4,4-ethylenedioxy-2-cyclopentenone resulted in formation of previously unknown 2,3-dichloro-4-hydroxy-4-[(Z)-2-octenyl]-2-cyclopentenone which is a universal block synthon for analogs of marine prostanoids.

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Authors and Affiliations

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

    P. P. Akhmetvaleev, G. M. Baibulatova, G. A. Shavaleeva & M. S. Miftakhov

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  1. P. P. Akhmetvaleev
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  2. G. M. Baibulatova
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  3. G. A. Shavaleeva
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  4. M. S. Miftakhov
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Akhmetvaleev, P.P., Baibulatova, G.M., Shavaleeva, G.A. et al. Prostanoids: LXXIV. 2,3-Dichloro- 4,4-ethylenedioxy-2-cyclopentenone in the Synthesis of Analogs of Marine Prostanoid. Russian Journal of Organic Chemistry 37, 40–45 (2001). https://doi.org/10.1023/A:1012365131512

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  • DOI: https://doi.org/10.1023/A:1012365131512

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