Abstract
The orientation of substituted amino groups around the double bond in 2,3-diaminopropenoates, versatile agents in the syntheses of heterocyclic systems, was determined in solution by NMR techniques. Nuclear Overhauser enhancement and long-range 13C–1H coupling constants were measured by NOESY or ROESY and HMBC experiments, respectively. © 1997 John Wiley & Sons, Ltd.
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