Ogaritte Yazbek on Muck Rack

Ogaritte Yazbek

As seen in: Royal Society of Chemistry
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Articles

Stereochemical matching determines both helix type and handedness in α/γ-peptides with a cyclic-constrained γ-amino acid

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By Dayi Liu, Ali Mansour Verified, Daoud Naoufal, Ogaritte Yazbek
| Royal Society of Chemistry Verified
Stereochemical matching determines both helix type and handedness in α/γ-peptides with a cyclic-constrained γ-amino acid The folding preferences of α/γ-peptides containing a bespoke chiral cyclobutane-constrained γ-amino acid have been examined in low-polarity solvent by quantum chemical calculations. With (S)-alanine the preferred conformation is a right-handed 12/10 helix, whereas with (R)-alanine a left-handed 12 helical architecture is promoted.
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