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Articles
Carboxamide versus sulfonamide in peptide backbone folding: A case study with a hetero foldamerPublished in
2013
DOI: 10.1021/ol4002762
PMID: 23473041
Volume: 15
Issue: 7
Pages: 1504 - 1507
Strikingly dissimilar hydrogen-bonding patterns have been observed for two sets of closely similar hetero foldamers containing carboxamide and sulfonamides at regular intervals. Although both foldamers maintain conformational ordering, the hydrogen-bonding pattern and backbone helical handedness differ diametrically. © 2013 American Chemical Society.
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About the journal
| Journal | Organic Letters |
|---|---|
| ISSN | 15237060 |
Authors (1)
Veera Venkata Ramesh E- Sophorolipid induced hydrothermal synthesis of Cu nanowires and its modulating effect on Cu nanostructures
- Switching the H-bonding network of a foldamer by modulating the backbone chirality and constitutional ratio of amino acids
- Carboxamide versus sulfonamide in peptide backbone folding: A case study with a hetero foldamer
- Carbohydrate-derived conformationally restricted bicyclic dipeptides as potential hetero foldamer building blocks
