Functionalization at C‐5 and at the C‐6 methyl group of 4‐methoxy‐6‐methyl‐2‐pyrone
- 1 January 1982
- journal article
- research article
- Published by Wiley in Journal of Heterocyclic Chemistry
- Vol. 19 (1) , 157-160
- https://doi.org/10.1002/jhet.5570190130
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.This publication has 18 references indexed in Scilit:
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