Issue 11, 1990

Reactivity of 2-methylene-1,3-dicarbonyl compounds. Inverse electron-demand Diels–Alder reactions with alkyl vinyl ethers

Abstract

Highly regioselective hetero-Diels–Alder reactions were achieved by reaction of 2-methyene-1,3-dicarbonyl compounds 1 with alkyl vinyl ethers 2. This regioselectivity of the cycloadditions was consistent with the results that could be predicted by considering the frontier orbital of 1.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 3041-3044

Reactivity of 2-methylene-1,3-dicarbonyl compounds. Inverse electron-demand Diels–Alder reactions with alkyl vinyl ethers

M. Yamauchi, S. Katayama, O. Baba and T. Watanabe, J. Chem. Soc., Perkin Trans. 1, 1990, 3041 DOI: 10.1039/P19900003041

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