Understanding the conformational behaviour of Ac-Ala-NHMe in different media. A joint NMR and DFT study?
Organic & Biomolecular Chemistry Pub Date: 2015-07-21 DOI: 10.1039/C5OB01296A
Abstract
The conformational behaviour of Ac-Ala-NHMe was studied in the gas-phase and in solution by theoretical calculations (B3LYP-D3/aug-cc-pVDZ level) and experimental 1H NMR. The conformational preferences of this compound were shown to result from a complex interplay between the strengths of possible intramolecular hydrogen bonds, steric interactions, hyperconjugation, entropy effects and the overall dipole moments. The Ac-Ala-N(Me)2 derivative was studied in addition, to design a system akin to Ac-Ala-NHMe, but with disrupted intramolecular hydrogen bonds involving the -NHMe group, mimicking the effect of polar protic solvents.
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Journal Name：Organic & Biomolecular Chemistry
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CAS no.: 89640-58-4
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