Synthesis and Anticancer Activity of 3-(3-Oxoprop-1-enyl)-Substituted Analogues of Carbocyclic Pyrimidine Nucleosides and 2′,3′-Dideoxy Pyrimidine Nucleosides-Reference-Cited by-同舟云学术

Synthesis and Anticancer Activity of 3-(3-Oxoprop-1-enyl)-Substituted Analogues of Carbocyclic Pyrimidine Nucleosides and 2′,3′-Dideoxy Pyrimidine Nucleosides

Published:1990-10 Issue:7 Volume:9 Page:923-935
ISSN:0732-8311
Container-title:Nucleosides and Nucleotides
language:en
Short-container-title:Nucleosides and Nucleotides

Author:

Lin Tai-Shun,Guo Ji-Yu,Zhang Xiao-Hui

Publisher

Informa UK Limited

Subject

Genetics,Biochemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/07328319008045209

Reference14 articles.

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2. Sartorelli, A. C. and Creasey, W. A. 1982.Cancer Medicine,, 2nd Edition, Edited by: Holland, J. F. and Frei, E. III. 720Philadelphia: Lea and Febiger.

3. Nucleic acid related compounds. 42. A general procedure for the efficient deoxygenation of secondary alcohols. Regiospecific and stereoselective conversion of ribonucleosides to 2'-deoxynucleosides

4. Acid-catalyzed cyclization of alkoxyacryloylureas to 2,4(1H,3H)pyrimidinediones

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