| Autor: |
Oleksandra Bugera, Zoia Voitenko, S. V. Shilin, Igor V. Levkov, O. V. Shablykina |
| Rok vydání: |
2019 |
| Předmět: |
|
| Zdroj: |
French-Ukrainian Journal of Chemistry. 7:111-119 |
| ISSN: |
2312-3222 |
| Popis: |
Through N-acylation of a- or b-amino acid units by 2-(3-oxo-2,3-dihydro-1H-inden-5-yloxy)acetic acid using the method of N-hydroxysuccinimide esters new dipeptide indan-1-one derivatives were obtained. In general, the direct interaction of the acetic carboxyl group of the substrate with the amino group of the a- or b-dipeptide is a more productive strategy than the sequential peptidic condensation of the two amino acids. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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