Incorporation of 2′-Deoxysangivamycin in DNA Duplexes: The Conversion of a Pyrrolo[2, 3-d]Pyrimidine Nitrile to a Carboxamide upon Oligonucleotide Deprotection
Author:
Affiliation:
1. a Laboratorium für Organische und Bioorganische Chemie, Institut für Chemie, Universität Osnabrück , Barbarastr. 7, D-49069 , Osnabrück , Germany
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328319908044635
Reference34 articles.
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1. ChemInform Abstract: Incorporation of 2′-Deoxysangivamycin in DNA Duplexes: The Conversion of a Pyrrolo[2,3-d]pyrimidine Nitrile to a Carboxamide upon Oligonucleotide Deprotection.;ChemInform;2010-06-08
2. Synthesis of Fluorinated Pyrrolo[2,3-b]pyridine and Pyrrolo[2,3-d]pyrimidine Nucleosides;Synthesis;2009-05-12
3. Facile Synthesis of Fluorinated Pyrrolo[2,3-b]pyridines;Synlett;2009-01-21
4. PROPYNYL GROUPS IN DUPLEX, HAIRPIN AND TRIPLEX DNA: 7-DEAZAPURINES AND 9-DEAZAPURINES;Nucleosides, Nucleotides & Nucleic Acids;2005-04-01
5. An Efficient Synthesis of Pyrrolo[2,3-d]pyrimidines via Inverse Electron Demand Diels−Alder Reactions of 2-Amino-4-cyanopyrroles with 1,3,5-Triazines;The Journal of Organic Chemistry;2002-11-01
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