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Volumn 29, Issue 6, 1996, Pages 1141-1155

Acyclic analogues of purine nucleosides: one- and two-dimensional 1H and 13C NMR evidences for N-9 and N-7 regioisomers

Author keywords

2D Homo and Heteronuclear Correlation Spectroscopy; 13C NMR; 1H NMR; Acyclonucleosides, Purine; Adenine; N 9 and N 7 regioisomers

Indexed keywords


EID: 0011284314     PISSN: 00387010     EISSN: None     Source Type: Journal    
DOI: 10.1080/00387019608007279     Document Type: Article
Times cited : (9)

References (13)
  • 1
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    • Antibiotics and Antiviral Agents
    • Krogsgaard-Larsen P. and Bundgaard H. eds. Chur: Harwood Academic Publishers
    • Vanderhaeghe H., Herdewijn P. and De Clercq E. Antibiotics and Antiviral Agents. In. Krogsgaard-Larsen P. and Bundgaard H. eds. A Textbook of Drug Design and Development, Chur: Harwood Academic Publishers: 1994: 577-605.
    • (1994) A Textbook of Drug Design and Development , pp. 577-605
    • Vanderhaeghe, H.1    Herdewijn, P.2    De Clercq, E.3
  • 4
    • 0011214014 scopus 로고
    • Acyclic and Carbocyclic Nucleoside Analogues as Inhibitors of HIV Replication
    • De Clercq E. ed. Amsterdam: Elsevier
    • De Clercq E. and Balzarini J. Acyclic and Carbocyclic Nucleoside Analogues as Inhibitors of HIV Replication. De Clercq E. ed. In: Design of anti AIDS Drugs, Amsterdam: Elsevier: 1990: 179-195.
    • (1990) Design of Anti AIDS Drugs , pp. 179-195
    • De Clercq, E.1    Balzarini, J.2
  • 5
    • 0026523623 scopus 로고
    • HIV Inhibitors Targeted at the Reverse Transcriptase
    • De Clercq E. HIV Inhibitors Targeted at the Reverse Transcriptase. AIDS Research Human Reterovirus, 1992; 8: 119-134.
    • (1992) AIDS Research Human Reterovirus , vol.8 , pp. 119-134
    • De Clercq, E.1
  • 7
    • 33748221082 scopus 로고
    • Regioselective Synthesis and Antiviral Activity of Purine Nucleoside Analogues with Acyclic Substituents at N7
    • Jähne G., Kroha H., Müller A., Helsberg M., Winkler I., Gross G., Scholl T. Regioselective Synthesis and Antiviral Activity of Purine Nucleoside Analogues with Acyclic Substituents at N7. Angew. Chem. Int. Ed. Engl., 1994; 33: 562-563.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 562-563
    • Jähne, G.1    Kroha, H.2    Müller, A.3    Helsberg, M.4    Winkler, I.5    Gross, G.6    Scholl, T.7
  • 9
    • 0016844473 scopus 로고
    • Carbon-13 Magnetic Resonance. XXV A Basic Set of Parameters for the Investigation of Tautomerism in Purines Established from Carbon-13 Magnetic Resonance Studies Using Certain Purines and Pyrrolo[2,3-d]pyrimidines
    • Chenon, M. T., Pugmire, R. J., Grant, D. M., Panzica, R. P., Townsend, L. B. Carbon-13 Magnetic Resonance. XXV A Basic Set of Parameters for the Investigation of Tautomerism in Purines Established from Carbon-13 Magnetic Resonance Studies Using Certain Purines and Pyrrolo[2,3-d]pyrimidines. J. Am. Chem. Soc., 1975; 97: 4627-4635.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 4627-4635
    • Chenon, M.T.1    Pugmire, R.J.2    Grant, D.M.3    Panzica, R.P.4    Townsend, L.B.5
  • 11
    • 0023272107 scopus 로고
    • Novel Acyclonucleosides. Part 2. 2,3-Dihydroxy-1-Methoxypropyl-Substituted Purines
    • Bailey, S. and Harnden, M. R. Novel Acyclonucleosides. Part 2. 2,3-Dihydroxy-1-Methoxypropyl-Substituted Purines Nucleosides & Nucleotides, 1987; 6: 555-574.
    • (1987) Nucleosides & Nucleotides , vol.6 , pp. 555-574
    • Bailey, S.1    Harnden, M.R.2
  • 13
    • 0001171156 scopus 로고
    • Purine Nucleosides. VIII. Reinvestigation of the Position of Glycosidation in Certain Synthetic "7"-Substituted 6-Dimethylaminopurine Nucleosides related to Puromycin
    • Townsend, L. B., Robins, R. K., Loeppky, R. N. and Leonard, N. J. Purine Nucleosides. VIII. Reinvestigation of the Position of Glycosidation in Certain Synthetic "7"-Substituted 6-Dimethylaminopurine Nucleosides related to Puromycin. J. Am. Chem. Soc., 1964; 86: 5320-5325.
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 5320-5325
    • Townsend, L.B.1    Robins, R.K.2    Loeppky, R.N.3    Leonard, N.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.