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NMR Studies of Substituted 2,3-Diaminopropenoates

✍ Scribed by Simona Golič Grdadolnik; Branko Stanovnik

Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
237 KB
Volume
35
Category
Article
ISSN
0749-1581

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✦ Synopsis

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

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