Methylenecyclopropane Analogues of Nucleosides: Synthesis, Absolute Configuration, and Enantioselectivity of Antiviral Effect of (R)-(-)- and (S)-(+)-Synadenol-Reference-Cited by-同舟云学术

Methylenecyclopropane Analogues of Nucleosides: Synthesis, Absolute Configuration, and Enantioselectivity of Antiviral Effect of (R)-(-)- and (S)-(+)-Synadenol

Published:1999-04 Issue:4-5 Volume:18 Page:597-598
ISSN:0732-8311
Container-title:Nucleosides and Nucleotides
language:en
Short-container-title:Nucleosides and Nucleotides

Author:

Qiu Y-L.,Hempel A.,Camerman N.,Camerman A.,Geiser F.,Ptak R. G.,Breitenbach J. M.,Kira T.,Li L.,Gullen E.,Cheng Y-C.,Drach J. C.,Zemlicka J.

Publisher

Informa UK Limited

Subject

Genetics,Biochemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/15257779908041507

Reference9 articles.

1. (Z)- and (E)-2-((Hydroxymethyl)cyclopropylidene)methyladenine and -guanine. New Nucleoside Analogues with a Broad-Spectrum Antiviral Activity

2. 3,5′-Anhydrosynadenol: A Polycyclic Anhydronucleoside Analogue

3. A New Efficient Synthesis of Antiviral Methylenecyclopropane Analogs of Purine Nucleosides

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5. Synthesis of (Z)- and (E)-9-[(2-Hydroxyethylidene)cyclopropyl]adenine—New Methylenecyclopropane Analogues of Adenosine and Their Substrate Activity for Adenosine Deaminase;Nucleosides, Nucleotides and Nucleic Acids;2000-01