A Facile One‐Pot Synthesis of N 4‐Alkyloxycarbonyl Cytosine Nucleosides
Author:
Affiliation:
1. a Department of Chemistry , Shanghai Institute of Pharmaceutical Industry , Shanghai, 200437, P.R. China
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1081/SCC-200030544
Reference13 articles.
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2. Synthesis and biological activity of the new 5-fluorocytosine derivatives, 5′-deoxy-N-alkyloxycarbonyl-5-fluorocytosine-5′-carboxylic acid
3. The design and synthesis of a new tumor-selective fluoropyrimidine carbamate, Capecitabine
4. Arasaki , M. N.R. Ishitsuka , H. Kuruma , I. Miwa , M. Murasaki , C. Shimma , N. and Umeda , I. I.H. N‐Oxycarbonyl‐substituted 5′‐deoxy‐5‐fluorocytidines as antitumor agents. EP 602,454. June 22, 1994.
5. Hertel , L. W. and Kroin , J. S. 2′‐Deoxy‐2′,2′‐difluoro‐(4‐substituted pyrimidine) nucleosides having antiviral and anti‐cancer activity and intermediates. EP 576,230. December 29, 1993.
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1. Recent Developments in the Use ofbis-(Trichloromethyl) Carbonate in Synthesis;Organic Preparations and Procedures International;2009-05-12
2. New Method of SynthesizingN‐Alkoxycarbonyl‐N‐arylamide with Triphosgene;Synthetic Communications;2006-09
3. A Facile One-Pot Synthesis of N4-Alkyloxycarbonyl Cytosine Nucleosides.;ChemInform;2005-02-15
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