Issue 2, 1990

Perkin communications. Heterocyclic [4++ 2] cycloadditions: the reactivity of pyridinium salts with electron-rich olefins

Abstract

The N-(2,4-dinitrophenyl) salts of N,N-diethylnicotinamide and ethyl nicotinate undergo [4++ 2] cycloaddition with enol ethers at room temperature, providing the first examples of Bradsher cyclization by monocyclic quaternary aza-aromatics; other derivatives and salts of pyridine are inert under these conditions.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 413-414

Perkin communications. Heterocyclic [4++ 2] cycloadditions: the reactivity of pyridinium salts with electron-rich olefins

J. R. Falck, S. J. Wittenberger, D. Rajapaksa, C. Mioskowski and B. Boubia, J. Chem. Soc., Perkin Trans. 1, 1990, 413 DOI: 10.1039/P19900000413

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