Chemistry of pyrones related to dehydroacetic acid. Functionalization at C‐5 and at the methyl group at C‐6. An attempted synthesis of a thromboxane B<inf>2</inf> analogue

R. Bacardit, J. Cervelló, P. de March, J. Marquet, M. Moreno‐Mañas, J. L. Roca

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Abstract

New derivatives of dehydroacetic acid and triacetic acid lactone functionalized at both C‐5 and at the methyl group at C‐6 have been synthesized as intermediates for the preparation of thromboxane B2 analogues. 6‐Mercaptomethyl‐4‐methoxy‐2‐pyrone and some derived thioethers have been also prepared. New thioether derivatives of O‐alkyloximes of dehydroacetic acid have been synthesized and tested for herbicidal activity. Copyright © 1989 Journal of Heterocyclic Chemistry
Original languageEnglish
Pages (from-to)1205-1212
JournalJournal of Heterocyclic Chemistry
Volume26
Issue number5
DOIs
Publication statusPublished - 1 Jan 1989

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