p-Methoxybenzyl as a NewN3-Imide Protecting Group of 5-Fluorouridine and Its Application to the Synthesis of 5′-O-Acryloyl-5-fluorouridine
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/19/3/19_3_339/_pdf
Reference10 articles.
1. 5-Fluorouracil derivatives. XVII. Synthesis and antitumor activity of 5'-O-acyl-5-fluorouridines.
2. Nucleosides. 114. 5'-O-Glucuronides of 5-fluorouridine and 5-fluorocytidine. Masked precursors of anticancer nucleosides
3. Die Synthese der 5′‐Diphosphate von 5‐Methyl‐uridin, 5‐Hydroxymethyl‐uridin und 3.5‐Dimethyl‐uridin
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1. Synthesis of a Complete Janus-type Guanosine–Cytosine Base and Its 2′-Deoxyribonucleoside;Chemistry Letters;2011-07-05
2. Efficient Preparation and Processing of the 4-Methoxybenzyl (PMB) Group for Phenolic Protection Using Ultrasound,;The Journal of Organic Chemistry;2008-06-13
3. p-Methoxybenzyl Chloride;Encyclopedia of Reagents for Organic Synthesis;2007-09-17
4. Novel and highly regioselective route for synthesis of 5-fluorouridine lipophilic ester derivatives by lipozyme TL IM;Journal of Biotechnology;2007-05
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