141282-52-2Relevant academic research and scientific papers
INFLUENCE OF THE INCORPORATION OF 1-(2,3-DIDEOXY-β-D-ERYTHRO-HEXOPYRANOSYL)-THYMINE ON THE ENZYMATIC STABILITY AND BASE-PAIRING PROPERTIES OF OLIGODEOXYNUCLEOTIDES
Augustyns, Koen,Aerschot, Arthur van,Urbanke, Claus,Herdewijn, Piet
, p. 119 - 130 (2007/10/02)
1-(2,3-Dideoxy-β-D-erythro-hexopyranosyl)thymine was used at several positions as nucleoside substitute in the synthesis of oligonucleotides using the H-phosphonate chemistry.A 13-mer with one hexose nucleoside substitution at each end had equivalent hybr
110. Warum Pentose- und nicht Hexose-Nucleinsaeuren? (Teil II) Oligonucleotide aus 2',3'-Dideoxy-β-D-glucopyranosyl-Bausteinen ('Homo-DNS'): Herstellung - Why Pentose and Not Hexose Nucleic Acids? Part II. Preparation of Oligonucleotides Containing 2',3'-
Boehringer, Markus,Roth, Hans-Joerg,Hunziker, Juerg,Goebel, Michael,Krishnan, Ravichandran,et al.
, p. 1416 - 1477 (2007/10/02)
This paper describes the preparation of the 2',3'-dideoxy-β-D-glucopyranosyl-(= 2',3'-dideoxy-β-D-erythro-hexapyranosyl)-derived nucleosides of the five bases adenine, cytosine, guanine, thymine, and uracil (= 'homo-deoxyribonucleosides') as well as the s
