Oligodeoxynucleotides Embodying the Ambiguous Base Z, 5-Amino-imidazole-4-carboxamide
Author:
Publisher
Informa UK Limited
Subject
Genetics,Biochemistry
Reference14 articles.
1. Kornberg, A and Baker, T. A., eds. 1992. “DNA replication”. NY: Freeman, W. H. and Company.
2. Synthesis and enzymatic polymerisation of 5-amino-1-(2′-deoxy-β-D-ribofuranosyl)imidazole-4-carboxamide-5′-triphosphate
3. Preparation of oligonucleotides containing dAICA using an unexpected side-reaction observed on a protected derivative of 2-aza-2′-deoxyinosine.
4. Studies in the Protection and Selective Deprotection of 5-Amino-1-β-D-Ribofuranosylimidazole-4-Carboxamide (Aica-Riboside)
5. The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups
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1. Synthesis and Behavior of DNA Oligomers Containing the Ambiguous Z-Nucleobase 5-Aminoimidazole-4-carboxamide;Molecules;2023-04-06
2. Synthesis of a Cyclic Dinucleotide Analogue with Ambiguous Bases, 5-Aminoimidazole-4-carboxamide;The Journal of Organic Chemistry;2021-10-15
3. 2-Substituted 2′-deoxyinosine 5′-triphosphates as substrates for polymerase synthesis of minor-groove-modified DNA and effects on restriction endonuclease cleavage;Organic & Biomolecular Chemistry;2020
4. Synthesis and incorporation into DNA fragments of the artificial nucleobase, 2-amino-8-oxopurine;Bioorganic & Medicinal Chemistry Letters;2005-02
5. Imidazole-4-Carboxamide and 1,2,4-Triazole-3-Carboxamide Deoxynucleotides as Simplified DNA Building Blocks with Ambiguous Pairing Capacity;Nucleosides and Nucleotides;1998-09
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