Issue 9, 1998

Regioselectivity in nucleophilic ring-opening of aziridinones

Abstract

The proportions of products derived from competing modes of ring-opening of 1,3-di-tert-butylaziridinone and similar aziridinones by a variety of nitrogen, oxygen, sulfur and halogen nucleophiles do not agree with simple guidelines postulated in the literature for these types of aziridinones.

Article information

Article type
Paper

Chem. Commun., 1998, 985-986

Regioselectivity in nucleophilic ring-opening of aziridinones

E. R. Talaty and M. M. Yusoff, Chem. Commun., 1998, 985 DOI: 10.1039/A800564H

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