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Original Articles

Synthetic Nucleoside and Nucleotides. XXXIV. Photoaffinity Labeling of HIV Reverse Transcriptase: Synthesis and Utilization of 2′,3′-Dideoxy Uridylate Analogs Bearing Aryl(trifluor0methyl)-Diazirine Moiety

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Pages 607-618 | Published online: 21 Aug 2006

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AndreyN. Topin, OxanaM. Gritsenko, MaximG. Brevnov, ElisavetaS. Gromova & GalinaA. Korshunova. (1998) Synthesis of a new Photo-Cross-Linking Nucleoside Analogue Containing an Aryl(Trifluoromethyl)Diazirine Group: Application for Eco RII and Mva I Restriction-Modification Enzymes. Nucleosides and Nucleotides 17:7, pages 1163-1175.
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Articles from other publishers (6)

Christine C. Smith, Marcel Hollenstein & Christian J. Leumann. (2014) The synthesis and application of a diazirine-modified uridine analogue for investigating RNA–protein interactions. RSC Adv. 4:89, pages 48228-48235.
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Anton Blencowe & Wayne Hayes. (2005) Development and application of diazirines in biological and synthetic macromolecular systems. Soft Matter 1:3, pages 178.
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Anatolii F Nasonov & Galina A Korshunova. (1999) C-Alkenylation of pyrimidine nucleosides and their analogues. Russian Chemical Reviews 68:6, pages 483-504.
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Serge L. Beaucage. 1999. Comprehensive Natural Products Chemistry. Comprehensive Natural Products Chemistry 153 249 .
T. Yamaguchi, K. Suyama, K. Narita, S. Kohgo, A. Tomikawa & M. Saneyoshi. (1997) Synthesis and evaluation of oligodeoxyribonucleotides containing an aryl(trifluoromethyl)diazirine moiety as the cross-linking probe: photoaffinity labeling of mammalian DNA polymerase  . Nucleic Acids Research 25:12, pages 2352-2358.
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T. YAMAGUCHI & M. SANEYOSHI. (2010) ChemInform Abstract: Synthetic Nucleoside and Nucleotides. Part 34. Photoaffinity Labeling of HIV Reverse Transcriptase: Synthesis and Utilization of 2′,3′‐ Dideoxy Uridylate Analogues Bearing Aryl(trifluoromethyl)diazirine Moiety.. ChemInform 27:25.
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