A new synthesis of the anti-AIDS drug AZT from 5-methyluridine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. An Efficient Synthesis of 3′-Azido-3′-deoxythymidine (AZT)
2. AIDS-driven nucleoside chemistry.
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Biocatalytic routes to anti-viral agents and their synthetic intermediates;Chemical Society Reviews;2021
2. IRMPD Action Spectroscopy, ER-CID Experiments, and Theoretical Studies of Sodium Cationized Thymidine and 5-Methyluridine: Kinetic Trapping During the ESI Desolvation Process Preserves the Solution Structure of [Thd+Na]+;Journal of the American Society for Mass Spectrometry;2017-08-23
3. Nucleosides with Modified Sugar Ring: Synthesis and Biological Activities;Current Organic Chemistry;2016-03-03
4. Two-step efficient synthesis of 5-methyluridine via two thermostable nucleoside phosphorylase from Aeropyrum pernix;Bioorganic & Medicinal Chemistry Letters;2012-03
5. Defining a process operating window for the synthesis of 5-methyluridine by transglycosylation of guanosine and thymine;Journal of Biotechnology;2011-01
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