Nucleosides and Nucleotides. 156. Chelation-Controlled and Nonchelation-Controlled Diastereofacial Selective Thiophenol Addition Reactions at the 2‘-Position of 2‘-[(Alkoxycarbonyl)methylene]-2‘-deoxyuridines: Conversion of (Z)-2‘-[(Alkoxycarbonyl)methylene]-2‘-deoxyuridines into Their (E)-Isomers1-Reference-Cited by-同舟云学术

Nucleosides and Nucleotides. 156. Chelation-Controlled and Nonchelation-Controlled Diastereofacial Selective Thiophenol Addition Reactions at the 2‘-Position of 2‘-[(Alkoxycarbonyl)methylene]-2‘-deoxyuridines: Conversion of (Z)-2‘-[(Alkoxycarbonyl)methylene]-2‘-deoxyuridines into Their (E)-Isomers1

Published:1997-01-01 Issue:1 Volume:62 Page:11-17
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hassan Abdalla E. A.¹,Shuto Satoshi¹,Matsuda Akira¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nishi-6, Kita-ku, Sapporo 060, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9613601

Reference26 articles.

1. Nucleosides and nucleotides. 155. synthesis, antitumor effects, and possible enzymatic activation mechanism of 5′-phosphatidyl-2′-deoxy-2′-methylenecytidine (DMDC)

2. Drug action on ribonucleotide reductase

3. (b) Mao, S. S.; Johnson, M. I.; Bollinger, J. M.; Baker, C. H.; Stubbe, J. InMolecular Mechanisms in Bioorganic Processes; Bleasdale, C., Goldman, B. T., Eds.; Royal Society of Chemistry: London, 1990, p 305.

4. Ribonucleotide Reductase and Cell Proliferation

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