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Site-selective solid phase synthesis of carbonylated peptides
The aim of our research was to design an efficient method for the solid phase synthesis of carbonylated peptides. For this purpose, we designed and synthesized a fully protected derivative Fmoc-amino(2,5,5-trimetyhyl-1,3-dioxolan-2-yl)acetic acid (Fmoc-Atda-OH) of a novel unnatural amino acid (Thr(O...
Tallennettuna:
| Julkaisussa: | Amino Acids |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Springer Vienna
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4458268/ https://ncbi.nlm.nih.gov/pubmed/25813939 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00726-015-1967-4 |
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