Issue 10, 1973

Rationale for the direction of regioselectivity in the photocycloaddition of arylazirines

Abstract

The photoconversion of substituted arylazirines (1) into methoxyimines (3) proceeds via a nitrile ylide intermediate (2); deuterium labelling results indicate that the electron density is highest on the disubstituted carbon atom of the nitrile ylide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1973, 342b-343

Rationale for the direction of regioselectivity in the photocycloaddition of arylazirines

A. Padwa and J. Smolanoff, J. Chem. Soc., Chem. Commun., 1973, 342b DOI: 10.1039/C3973000342B

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