Ontology highlight
ABSTRACT:
SUBMITTER: Siebler C
PROVIDER: S-EPMC6090429 | biostudies-literature | 2015 Dec
REPOSITORIES: biostudies-literature
Siebler Christiane C Maryasin Boris B Kuemin Michael M Erdmann Roman S RS Rigling Carla C Grünenfelder Claudio C Ochsenfeld Christian C Wennemers Helma H
Chemical science 20150812 12
NMR spectroscopic studies with a series of proline derivatives revealed that the polarity of the environment has a significant effect on the <i>trans</i> : <i>cis</i> isomer ratio of Xaa-Pro bonds. Computational studies showed that this effect is due to differences in the overall dipole moments of <i>trans</i> and <i>cis</i> conformers. Comparisons between the conformational properties of amide and ester derivatives revealed an intricate balance between polarity effects and n → π* interactions o ...[more]