Issue 13, 1998
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Cycloadditions of 6H-1,3,4-oxadiazin-6-ones (4,5-diaza-α-pyrones). Part 16.1 4-Substituted and 4,5-disubstituted methyl 3-phenyl-α-pyrone-6-carboxylates from γ-oxoketenes via α,δ-dibromo-δ-lactones

Thomas T. Tidwell,   Frank Sammtleben  and  Manfred Christl  

Abstract

The addition of bromine to the γ-oxoketenes 4, 10 and 22 and the elimination of two equivalents of hydrogen bromide from the resulting α,δ-dibromo-δ-lactones 5, 12 and 23 to give the α-pyrones 7, 19 and 20, respectively, are described. Since the isolation of neither 4, 10 and 22 nor 5, 12 and 23 proved necessary, the α-pyrones have been prepared in one-pot procedures from methyl 6-oxo-5-phenyl-6H-1,3,4-oxadiazine-2-carboxylate 6.

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Article information

DOI
https://doi.org/10.1039/A802364F
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 2031-2036

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Cycloadditions of 6H-1,3,4-oxadiazin-6-ones (4,5-diaza-α-pyrones). Part 16.1 4-Substituted and 4,5-disubstituted methyl 3-phenyl-α-pyrone-6-carboxylates from γ-oxoketenes via α,δ-dibromo-δ-lactones

T. T. Tidwell, F. Sammtleben and M. Christl, J. Chem. Soc., Perkin Trans. 1, 1998, 2031 DOI: 10.1039/A802364F

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