Conformational analysis of a model synthetic prodiginine.

Abstract

A conformational analysis of a synthetic model prodiginine was carried out. In solution this compound showed a strong preference for the β conformation, in which all the heterocycles are mutually cis. This conformation provided an ideal alignment of the three N-H groups for interacting with anions when the molecule is protonated. A different conformation… (More)
DOI: 10.1021/jo301008c

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Cite this paper

@article{GarcaValverde2012ConformationalAO, title={Conformational analysis of a model synthetic prodiginine.}, author={Mar{\'i}a Garc{\'i}a-Valverde and Ignacio Alfonso and David Qui{\~n}onero and Roberto Quesada}, journal={The Journal of organic chemistry}, year={2012}, volume={77 15}, pages={6538-44} }