The Synthesis of Amino Acid Methyl Ester 5′-Phosphoamidates of Protected Uridine-Reference-Cited by-同舟云学术

The Synthesis of Amino Acid Methyl Ester 5′-Phosphoamidates of Protected Uridine

Published:2010-09-24 Issue:10 Volume:185 Page:2054-2063
ISSN:1042-6507
Container-title:Phosphorus, Sulfur, and Silicon and the Related Elements
language:en
Short-container-title:Phosphorus, Sulfur, and Silicon and the Related Elements

Author:

Chen W. Z.¹²,Zhao Y. F.¹³

Affiliation:

1. a Department of Chemistry and Key Laboratory for Chemical Biology of Fujian Province , Xiamen University , Xiamen, China

2. b The Third Institute of Oceanography of the State Oceanic Administration , Xiamen, China

3. c Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry , Tsinghua University , Beijing, China

Publisher

Informa UK Limited

Subject

Inorganic Chemistry,Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10426500903490237

Reference17 articles.

1. Carbocyclic Analogs of Arabinosylpurine Nucleosides

2. Synthesis and biological evaluation of carbocyclic analogs of lyxofuranosides of 2-amino-6-substituted purines and 2-amino-6-substituted-8-azapurines

3. Synthesis and antiviral activity of carbocyclic analogs of 2'-deoxyribofuranosides of 2-amino-6-substituted-purines and of 2-amino-6-substituted-8-azapurines

4. Aromatic amino acid phosphoramidate di- and triesters of 3′-azido-3′-deoxythymidine (AZT) are non-toxic inhibitors of HIV-1 replication

5. Differential Patterns of Intracellular Metabolism of 2′,3′-Didehydro-2′,3′-dideoxythymidine and 3′-Azido-2′,3′-dideoxythymidine, Two Potent Anti-human Immunodeficiency Virus Compounds

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