Synthesis and characterization of new acyclic nucleosides analogues derived from 2-phenyl quinoline candidates
- 作者: Khalifa N.1,2, Al-Omar M.1,3, Amr A.3,4
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隶属关系:
- Pharmaceutical Chemistry Department, Drug Exploration and Development Chair, College of Pharmacy
- Department of Therapeutical Chemistry, Pharmaceutical and Drug Industries Division
- Pharmaceutical Chemistry Department, College of Pharmacy
- Applied Organic Chemistry Department
- 期: 卷 86, 编号 5 (2016)
- 页面: 1115-1119
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/215000
- DOI: https://doi.org/10.1134/S1070363216050224
- ID: 215000
如何引用文章
详细
Reaction of 4-substituted quinoline hydrazide with some aldohexoses and aldopentoses gave a series of new N-β-glycosides. The following cyclization of N-β-glycosides with acetic anhydride led to O-acetyl-[5-(2-phenylquinolin-4-yl)-1,3,4-oxadiazol-2-yl]-D-glycosides. Structure of the newly synthesized products was elucidated by chemical and spectroscopic methods.
作者简介
N. Khalifa
Pharmaceutical Chemistry Department, Drug Exploration and Development Chair, College of Pharmacy; Department of Therapeutical Chemistry, Pharmaceutical and Drug Industries Division
编辑信件的主要联系方式.
Email: nagykhalifa@hotmail.com
沙特阿拉伯, Riyadh, 11451; Dokki, Cairo, 12622
M. Al-Omar
Pharmaceutical Chemistry Department, Drug Exploration and Development Chair, College of Pharmacy; Pharmaceutical Chemistry Department, College of Pharmacy
Email: nagykhalifa@hotmail.com
沙特阿拉伯, Riyadh, 11451; Riyadh, 11451
A. Amr
Pharmaceutical Chemistry Department, College of Pharmacy; Applied Organic Chemistry Department
Email: nagykhalifa@hotmail.com
沙特阿拉伯, Riyadh, 11451; Dokki, Cairo, 12622
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