Synthesis of 2′,3′-Dideoxypurinenucleosides via the Palladium Catalyzed Reduction of 9-(2,5-Di-O-acetyl-3-bromo-3-deoxy-β-d-xylofuranosyl)purine Derivatives-Reference-Cited by-同舟云学术

Synthesis of 2′,3′-Dideoxypurinenucleosides via the Palladium Catalyzed Reduction of 9-(2,5-Di-O-acetyl-3-bromo-3-deoxy-β-d-xylofuranosyl)purine Derivatives

Published:1996-01 Issue:1-3 Volume:15 Page:31-45
ISSN:0732-8311
Container-title:Nucleosides and Nucleotides
language:en
Short-container-title:Nucleosides and Nucleotides

Author:

Shiragami Hiroshi¹,Amino Yusuke¹,Honda Yutaka¹,Arai Masayuki¹,Tanaka Yasuhiro¹,Iwagami Hisao¹,Yukawa Toshihide¹,Izawa Kunisuke¹

Affiliation:

1. a Central Research Laboratories, Ajinomoto Co., Inc. , 1-1, Suzuki-cho, Kawasaki-ku, Kawasaki , 210 , Japan

Publisher

Informa UK Limited

Subject

Genetics,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/07328319608002368

Reference35 articles.

1. 3'-Azido-3'-deoxythymidine (BW A509U): an antiviral agent that inhibits the infectivity and cytopathic effect of human T-lymphotropic virus type III/lymphadenopathy-associated virus in vitro.

2. 3'-Azido-3'-deoxythymidine (BW A509U): an antiviral agent that inhibits the infectivity and cytopathic effect of human T-lymphotropic virus type III/lymphadenopathy-associated virus in vitro.

3. Inhibition of the in vitro infectivity and cytopathic effect of human T-lymphotrophic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV) by 2',3'-dideoxynucleosides.

4. Broad spectrum antiretroviral activity of 2',3'-dideoxynucleosides.

5. Potential anti-AIDS drugs. 2',3'-Dideoxycytidine analogs

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1. ChemInform Abstract: Synthesis of 2′,3′-Dideoxypurinenucleosides via the Palladium Catalyzed Reduction of 9-(2,5-Di-O-acetyl-3-bromo-3-deoxy-β-D- xylofuranosyl)purine Derivatives.;ChemInform;2010-08-05

2. Synthesis of 2′,3′-Dideoxyinosine via Radical Deoxygenation;Nucleosides, Nucleotides & Nucleic Acids;2007-11-26

3. Synthesis of 2,3-Didehydro-2,3-dideoxynucleosides via Nucleoside Route.;Current Organic Synthesis;2006-08-01

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