Conformation of Cyclolinopeptide A Observed by Circular Dichroism
A stereochemical investigation, by circular dichroism, of a synthetic nonapeptide (cyclolinopeptide A) in several organic and organic-sulfuric acid solvents is presented. From this examination, and results found for a conformationally rigid model compound, 1,7,7-trimethyl-3-azabicyclo [2.2.1] heptan...
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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
1971
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC389152/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/16591927/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.68.6.1195 |
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