Regioselektive Synthese und antivirale Wirksamkeit von an N7 acyclisch substituierten Purinnucleosid‐Analoga
Authors:
- Gerhard GrossGGGerhard Gross
- Thomas SchollTSThomas Scholl
- 3 March 1994
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 106 (5) , 603-605
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Preparative Electrochemical Reduction of 2-Amino-6-chloropurine and Synthesis of 6-Deoxyacyclovir, a Fluorescent Substrate of Xanthine Oxidase and a Prodrug of Acyclovir.Acta Chemica Scandinavica, 1987
- Chemistry and antiviral activities of acyclonucleosidesJournal of Heterocyclic Chemistry, 1986
- Synthesis and antiherpetic activity of (S)-, (R)-, and (.+-.)-9-[(2,3-dihydroxy-1-propoxy)methyl]guanine, linear isomers of 2'-nor-2'-deoxyguanosineJournal of Medicinal Chemistry, 1985
- Synthesis of antiviral compounds. Preparation and rearrangement of 6-methoxyglyceropurinesCanadian Journal of Chemistry, 1984
- Synthesis of a purine acyclonucleoside series having pronounced antiviral activity. The glyceropurinesCanadian Journal of Chemistry, 1984
- 9-(1,3-Dihydroxy-2-propoxymethyl)guanine: a new potent and selective antiherpes agentJournal of Medicinal Chemistry, 1983
- Biologically active acyclonucleoside analogues. II. The synthesis of 9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]guanine (BIOLF-62)Canadian Journal of Chemistry, 1982
- Activation by thymidine kinase and potent antiherpetic activity of 2′-nor-2′-deoxyguanosine (2′NDG)Biochemical and Biophysical Research Communications, 1982
- 9-(2-Hydroxyethoxymethyl)guanine activity against viruses of the herpes groupNature, 1978
- Selectivity of action of an antiherpetic agent, 9-(2-hydroxyethoxymethyl)guanineProceedings of the National Academy of Sciences, 1977