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2'-deoxyaristeromycin

Known as: Cyclopentanemethanol, 4-(6-amino-9H-purin-9-yl)-2-hydroxy-, (1R-(1alpha,2beta,4alpha))- 
National Institutes of Health

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Broader (1)

Deoxyadenosines

Papers overview

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2001
2001
The First Example of a Hoogsteen Basepaired DNA Duplex in Dynamic Equilibrium with a Watson-Crick Basepaired Duplex—A Structural (NMR), Kinetic and Thermodynamic Study
Abstract A single-point substitution of the O4′ oxygen by a CH2 group at the sugar residue of A 6 (i.e. 2′-deoxyaristeromycin… 
1999
1999
A single carbocyclic nucleotide substitution in a 12mer DNA gives a Hoogsteen basepaired duplex (till 38 degrees C) and a hairpin (till 65 degrees C). A 600 MHz NMR spectroscopic study.
The impact of intramolecular stereoelectronic effects has been examined by comparison of the solution structures of natural oligo… 
1998
1998
Synthesis of enzymatically noncleavable carbocyclic nucleosides for DNA-N-glycosylase studies.
Carbocyclic nucleosides have been of great interest as antiviral agents and in studies in the area of antisense technology. The… 
1985
1985
Protected 2'-deoxyaristeromycin on polymer support: a substitute for the acid labile 2'-deoxyadenosine moiety at the 3'-terminus of oligodeoxynucleotides.
A modified nucleoside antibiotic on polymer support was employed in the solid-phase synthesis of two oligodeoxynucleotides to… 
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