Stereospecific synthesis and antiviral properties of different enantiomerically pure carbocyclic 2'-deoxyribonucleoside analogs derived from common chiral pools: (+)-(1R,5S)- and (-)-(1S,5R)-2-oxabicyclo[3.3.0]oct-6-en-3-one-Reference-Cited by-同舟云学术

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Stereospecific synthesis and antiviral properties of different enantiomerically pure carbocyclic 2'-deoxyribonucleoside analogs derived from common chiral pools: (+)-(1R,5S)- and (-)-(1S,5R)-2-oxabicyclo[3.3.0]oct-6-en-3-one

Published:1990-05 Issue:5 Volume:33 Page:1353-1360
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Beres J.,Sagi G.,Tomoskozi I.,Gruber L.,Baitz-Gacs E.,Otvos L.,De Clercq E.

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm00167a011

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1. Stereoselective Synthesis ofD- andL-Carbocyclic Nucleosides by Enzymatically Catalyzed Kinetic Resolution;Chemistry - A European Journal;2012-07-24

2. Highlights in Antiviral Drug Research: Antivirals at the Horizon;Medicinal Research Reviews;2012-05-02

3. Some Synthetic Uses of Halides;PATAI'S Chemistry of Functional Groups;2009-12-15

4. Carbocyclic Thymidine Analogues for Use as Potential Therapeutic Agents;Nucleosides, Nucleotides & Nucleic Acids;2009-07-29

5. Facile synthesis of 9-(N-amino-4-fluoromethyl-3-pyrrolidinyl)-2-fluoro-6-aminopurine from trans-4-hydroxy-l-proline;Chinese Chemical Letters;2007-11

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