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In this paper we report the synthesis and the conformational analysis of several acyclic N-cyanoamides based molecules as new conformational probes. The conformational behavior and the stability of these molecules has been investigated in solution by 1H and 31P NMR spectroscopy. For all these compounds a conformational equilibrium between A- (gauche-gauche) and E- (gauche-trans) arrangement has been found. Moreover, we show that in solution, the conformational behavior of acyclic N-cyanoamides is similar to that of 2-acyliminocyclopentan-2-amides. Indeed, since acyclic imines derivatives do not have the intramolecular hydrogen bond as 2-acyliminocyclopentan-2-amides, a conformational equilibrium between gauche-gauche and gauche-trans arrangement can be observed in these molecules as well. Indeed, NMR analysis of acyclic imines has confirmed this hypothesis. The conformational behavior of five acyclic N-cyanoamides has been also investigated by molecular modeling calculations. Molecular dynamics calculations have
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