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Asymmetric synthesis of propargylamines as amino acid surrogates in peptidomimetics
The amide moiety of peptides can be replaced for example by a triazole moiety, which is considered to be bioisosteric. Therefore, the carbonyl moiety of an amino acid has to be replaced by an alkyne in order to provide a precursor of such peptidomimetics. As most amino acids have a chiral center at...
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| Publicado en: | Beilstein J Org Chem |
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| Main Authors: | , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Beilstein-Institut
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5704752/ https://ncbi.nlm.nih.gov/pubmed/29234470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.13.240 |
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