153527-31-2Relevant academic research and scientific papers
Expansion of repertoire of modified DNAs prepared by PCR using KOD Dash DNA polymerase
Ohbayashi, Tsutomu,Kuwahara, Masayasu,Hasegawa, Masatoshi,Kasamatsu, Toshiyuki,Tamura, Takehiro,Sawai, Hiroaki
, p. 2463 - 2468 (2005)
Thymidine analogues bearing a variety of functional groups at the C5-position via an amino-linker arm were prepared and the substrate activity for PCR using thermophilic KOD Dash DNA polymerase was examined. The enzyme accepted the thymidine analogues bea
Reagents for addressed modification of biopolymers 11. The synthesis of NIm-2,4-dinitrophenyl derivatives of histidine and urocanic and imidazolylacetic acids for anchoring imidazole residues to oligonucleotides
Karyagin,Abramova,Sil'nikov,Shishkin
, p. 540 - 545 (2007/10/03)
Derivatives of histidine, imidazolylacetic and urocanic acids, containing an NIm-2,4-dinitrophenyl moiely and a hydroxy group were synthesized and characterized. The applicability of these reagents for anchoring imidazole residues to oligonucle
Synthesis of oligonucleotides containing N2-2-(imidazol-4-ylacetamido)ethyll-2′-deoxyguanosine
Wang, Guangyi,Bergstrom, Donald E.
, p. 6725 - 6728 (2007/10/02)
Synthesis of 2′-deoxyguanosine tethered through N-2 to an imidazole is described. The modified 2′-deoxyguanosine was converted to two different phosphoramidites, one with and the other without a 6-O-protecting group. The phosphoramidites were incorporated
