Synthesis of carboxamide linked dimers, αT*αT and αUCl*αT. — duplex and triplex stabilities of the corresponding α oligodeoxynucleotides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Α-DNA II. Synthesis of unnatural Α-anomeric oligodeoxyribonucleotides containing the four usual bases and study of their substrate activities for nucleases
2. α-Oligodeoxynucleotide stability in serum, subcellular extracts and culture media
3. α-DNA-V. Parallel annealing, handedness and conformation of the duplex of the unnatural α-hexadeoxyribonucleotide α-[d(CpApTpGpCpG)] with its β-complement β-[d(GpTpApCpGpC)] deduced from high field1H-NMR
4. α-DNA VI: comparative study of α- and β-anomeric oligodeoxyribonucleotides in hybridization to mRNA and in cell free translation inhibition
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1. Donor/acceptor chromophores-decorated triazolyl unnatural nucleosides: synthesis, photophysical properties and study of interaction with BSA;Organic & Biomolecular Chemistry;2016
2. From Anionic to Cationicα-Anomeric Oligodeoxynucleotides;Chemistry & Biodiversity;2010-03
3. Improved Targeting of the Flanks of a DNA Stem Using α-Oligodeoxynucleotides.-The Enhanced Effect of an Intercalator;Nucleosides and Nucleotides;1998-12
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