Issue 13, 1984

An e.s.r. study of the ring opening of 2-methylaziridine-boryl radicals

Abstract

The cis-isomer of the 2-methylaziridine-boryl radical undergoes ring opening with C–N cleavage to give mainly the secondary alkyl radical, while the trans-isomer gives mainly the less stable primary alkyl radical.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 850-852

An e.s.r. study of the ring opening of 2-methylaziridine-boryl radicals

J. A. Baban and B. P. Roberts, J. Chem. Soc., Chem. Commun., 1984, 850 DOI: 10.1039/C39840000850

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