PROPYNYL GROUPS IN DUPLEX, HAIRPIN AND TRIPLEX DNA: 7-DEAZAPURINES AND 9-DEAZAPURINES
Author:
Affiliation:
1. a Laboratorium für Organische und Bioorganische Chemie , Institut für Chemie, Universität Osnabrück , Osnabrück, Germany
2. b Center for Nanotechnology (CeNTech) , Munster, Germany
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1081/NCN-200059184
Reference7 articles.
1. Propynyl groups in duplex DNA: stability of base pairs incorporating 7-substituted 8-aza-7-deazapurines or 5-substituted pyrimidines
2. Oligodeoxynucleotides containing C-7 propyne analogs of 7-deaza-2'- deoxyguanosine and 7-deaza-2'-deoxyadenosine
3. Duplex Stability of 7-Deazapurine DNA: Oligonucleotides containing 7-bromo- or 7-iodo-7-deazaguanine
4. Incorporation of 2′-Deoxysangivamycin in DNA Duplexes: The Conversion of a Pyrrolo[2, 3-d]Pyrimidine Nitrile to a Carboxamide upon Oligonucleotide Deprotection
5. Design of an N7-Glycosylated Purine Nucleoside for Recognition of GC Base Pairs by Triple Helix Formation
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1. Synthesis of N7-Alkyl-9-deaza-2′-deoxyguanosines Containing Polar N7 Chains. Examples of Chemically Stable Analogues of N7-Hydroxyethyl and N7-Oxoethyl Adducts of 2′-Deoxyguanosine;The Journal of Organic Chemistry;2016-11-17
2. C-Functionalization of 9-deazapurines by cross-coupling reactions;Tetrahedron;2007-02
3. Nucleotides and nucleic acids; oligo- and polynucleotides;Organophosphorus Chemistry
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