Issue 4, 1982

Reverse orientation in the 1,3-dipolar cycloaddition of some pyridinium betaines to unsymmetrical alkenes

Abstract

Analysis of the products formed by the addition of N-phenylpyridium betaines to some unsymmetrical alkenes revealed that the 2-methyl-or-mehtyl-or 2-phenyl-N-phenylpyridinium betaine tends to form the reverse orientation products, whereas the unsubstituted N-phenylpyridium betaine gives the expected orientation.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 262-263

Reverse orientation in the 1,3-dipolar cycloaddition of some pyridinium betaines to unsymmetrical alkenes

M. Hamaguchi, H. Matsuura and T. Nagai, J. Chem. Soc., Chem. Commun., 1982, 262 DOI: 10.1039/C39820000262

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