Structure and Nuclear Magnetic Resonance Spectrum of N-Nitrosocamphidine

Abstract
The 220 MHz n.m.r. spectrum of N-nitrosocamphidine is interpreted in terms of a 1:1 syn-anti isomer mixture. Benzene solvent-induced shifts and the spectrum of the tris(dipivalomethanato)europium(III) – nitrosocamphidine complex are used to assign the methyl resonances.

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