Application of the Knorr reaction for the directional synthesis of pyrazole derivative as a biologically active co-ligandes of gold glyco-nanoparticles
- 作者: Ershov A.Y.1, Martynenkov A.A.1, Lagoda I.V.2, Batyrenko A.A.2
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隶属关系:
- Institute of Macromolecular Compounds of Russian Academy of Sciences
- State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation
- 期: 卷 59, 编号 11 (2023)
- 页面: 1489-1491
- 栏目: Articles
- URL: https://aspvestnik.ru/0514-7492/article/view/667142
- DOI: https://doi.org/10.31857/S0514749223110101
- EDN: https://elibrary.ru/NCKVEC
- ID: 667142
如何引用文章
详细
Based on the reaction of acetylacetone with 6-mercaptohexanoic and 11-mercaptoundecanoic acid hydrazides, a method was developed for the synthesis of previously unknown 1-(ω-mercaptoacyl)-3,5-dimethylpyrazole as promising сo-ligand for the preparation of gold glyco-nanoparticles for biomedical purposes.
作者简介
A. Ershov
Institute of Macromolecular Compounds of Russian Academy of Sciences
Email: ershov305@mail.ru
A. Martynenkov
Institute of Macromolecular Compounds of Russian Academy of Sciences
I. Lagoda
State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation
A. Batyrenko
State Research Testing Institute of Military Medicine, Ministry of Defense of the Russian Federation
参考
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