Condensation Approach to Aliphatic Oligourea Foldamers: Helices with N‐(Pyrrolidin‐2‐ylmethyl)ureido Junctions
Identifieur interne : 002574 ( Main/Exploration ); précédent : 002573; suivant : 002575Condensation Approach to Aliphatic Oligourea Foldamers: Helices with N‐(Pyrrolidin‐2‐ylmethyl)ureido Junctions
Auteurs : Juliette Fremaux [France] ; Lucile Fischer [France] ; Thomas Arbogast [France] ; Brice Kauffmann [France] ; Gilles Guichard [France]Source :
- Angewandte Chemie International Edition [ 1433-7851 ] ; 2011-11-25.
English descriptors
- Teeft :
- Aliphatic oligourea foldamers, Aliphatic oligoureas, Angew, Chem, Convergent condensation, Crystal structures, Foldamers, Guichard, Helical, Helical structure, Helix, Long helical segments, Main chain, Oligourea foldamers, Oligoureas, Proline, Proline residues, Pyrrolidine, Pyrrolidine junction, Pyrrolidine ring, Pyrrolidine unit, Pyrrolidine units, Segment junctions, Short oligoureas, Succinimidyl carbamate, Urea, Verlag gmbh, Weinheim angew.
Abstract
Caught in a fold: A simple and efficient coupling strategy to make aliphatic oligourea foldamers is reported. Crystal structures show that the pyrrolidine units (red; see picture) do not impair the 2.5‐helical folding of the oligoureas. This modular strategy enables assembly of long helical segments containing non‐adjacent pyrrolidine units as exemplified by the synthesis of a helix that is approximately 40 Å long.
Url:
DOI: 10.1002/anie.201105416
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Caught in a fold: A simple and efficient coupling strategy to make aliphatic oligourea foldamers is reported. Crystal structures show that the pyrrolidine units (red; see picture) do not impair the 2.5‐helical folding of the oligoureas. This modular strategy enables assembly of long helical segments containing non‐adjacent pyrrolidine units as exemplified by the synthesis of a helix that is approximately 40 Å long.</div>
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