Functionalization at C‐5 and at the C‐6 methyl group of 4‐methoxy‐6‐methyl‐2‐pyrone

R. Bacardit, M. Moreno‐Mañas, R. Pleixats

Research output: Contribution to journalArticleResearchpeer-review

23 Citations (Scopus)

Abstract

A new entry to C‐5 substituted 4‐hydroxy‐6‐methyl‐2‐pyrones has been achieved. The best conditions to prepare the monobromo and the dibromo derivatives at C‐3 and the C‐6 methyl group of the title pyrone have been defined. The synthetic applicability of the phosphonium salts at CH3‐C‐6 of both 4‐methoxy‐6‐methyl‐2‐pyrone, 5, and dehydroacetic acid, 2, has also been evaluated. Copyright © 1982 Journal of Heterocyclic Chemistry
Original languageEnglish
Pages (from-to)157-160
JournalJournal of Heterocyclic Chemistry
Volume19
Issue number1
DOIs
Publication statusPublished - 1 Jan 1982

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