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Conformational Preferences of β– and γ–Aminated Proline Analogues
Quantum mechanical calculations have been used to investigate how the incorporation of an amino group to the C(β)- or C(γ)-positions of the pyrrolidine ring affects the intrinsic conformational properties of the proline. Specifically, a conformational study of the N-acetyl-N′-methylamide derivatives...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2836598/ https://ncbi.nlm.nih.gov/pubmed/18842022 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jp807638p |
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