## Abstract Two conformers of fosinopril sodium in methanol were unambiguously established using 2D NMR methods and variable‐temperature NMR experiments. Differences in their conformational structure were shown to be related to the rotational energy barrier about the amide bond and hydrophobic inte
Approach to the conformational behaviour of tetraazamacrocycles in the solution state. NMR and molecular modelling studies
✍ Scribed by R. Boetzel; S. Failla; P. Finocchiaro; G. Hägele
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 537 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The differences in complexation behaviour of two diastereomeric tetraazamacrocycles, meso (1) and racemic (2) 5,5,7,12,12,14‐hexamethyl‐1,4,8,11‐tetraazacyclotetradecane, are explained by different conformations in solution, 1 being one stable conformer of almost rigid structure while 2 shows higher conformational flexibility to avoid steric strain. The methods used were ^1^H and ^13^C NMR and molecular modelling.
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