Convenient Synthesis of 2′-Deoxy-2-fluoroadenosine from 2-Fluoroadenine-Reference-Cited by-同舟云学术

Convenient Synthesis of 2′-Deoxy-2-fluoroadenosine from 2-Fluoroadenine

Published:2003-10-01 Issue:10 Volume:22 Page:1899-1905
ISSN:1525-7770
Container-title:Nucleosides, Nucleotides & Nucleic Acids
language:en
Short-container-title:Nucleosides, Nucleotides & Nucleic Acids

Author:

Ye Song¹,Rezende Martha M.¹,Deng Wei-Ping¹,Kirk Kenneth L.¹²

Affiliation:

1. a Laboratory of Bioorganic Chemistry , National Institute of Diabetes, and Digestive and Kidney Diseases, National Institutes of Health, DHHS , Bethesda, Maryland, USA

2. b Laboratory of Bioorganic Chemistry , National Institute of Diabetes, and Digestive and Kidney Diseases, National Institutes of Health, DHHS , Bethesda, MD, 20892, USA

Publisher

Informa UK Limited

Subject

Genetics,Molecular Medicine,Biochemistry,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1081/NCN-120025237

Reference6 articles.

1. Antitumor activity of 2-fluoro-2′-deoxyadenosine against tumors that express Escherichia coli purine nucleoside phosphorylase

2. Metabolism and Metabolic Actions of 6-Methylpurine and 2-Fluoroadenine in Human Cells

3. Nucleosides of 2-Fluoroadenine

4. A Convenient Synthesis of 2′-Deoxy-2-fluoroadenosine; a Potential Prodrug for Suicide Gene Therapy

5. Stereoselective Synthesis of 2'-Deoxy-.beta.-D-threo-pentofuranosyl Nucleosides by the NBS-Promoted Coupling Reaction of Thioglycosides with Silylated Heterocyclic Bases

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