Title of article :
Efficient synthesis of functionalized oligodeoxyribonucleotides with base-labile groups using a new silyl linker Original Research Article
Author/Authors :
Akihiro Ohkubo، نويسنده , , Rintaro Kasuya، نويسنده , , Katsufumi Aoki، نويسنده , , Akio Kobori، نويسنده , , Haruhiko Taguchi، نويسنده , , Kohji Seio، نويسنده , , Mitsuo Sekine، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
7
From page :
5345
To page :
5351
Abstract :
In this study, we developed new 3′-terminal deoxyribonucleoside-loading reagents 1 with a new silyl-type linker. These reagents could increase the efficiency of introduction of 3′-terminal deoxyribonucleoside components into polymer supports to a level of 17–29 μmol/g. The efficiency was higher than that of previous T-loading reagents because reagents 1 contain a 4-aminobutyryl residue as a spacer. Moreover, we could synthesize not only unmodified DNA oligomers but also a base-labile modified DNA oligomer using resins 9a–d in the activated phosphite method without base protection.
Keywords :
Silyl linker , DNA synthesis , N-unprotected phosphoramidite approach , Solid-phase synthesis
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2008
Journal title :
Bioorganic and Medicinal Chemistry
Record number :
1304346
Link To Document :
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