658712-92-6Relevant academic research and scientific papers
Large stabilization of a DNA duplex by the deoxyadenosine derivatives tethering an aromatic hydrocarbon group
Nakano, Shu-ichi,Uotani, Yuuki,Nakashima, Shoji,Anno, Yosuke,Fujii, Masayuki,Sugimoto, Naoki
, p. 8086 - 8087 (2003)
Novel deoxyadenosine derivatives tethering a phenyl or naphthyl group by means of an amido linker have been synthesized, and these derivatives, stacking on the 5′ end of a DNA duplex, provide free energy contributions equal to or greater than that of the
Molecular recognition of cationic phenothiazinium and phenoxazinium dyes with π-extended 2'-deoxyadenosine nucleotides
Mondragon-Vasquez, Karina,Morales-Rojas, Hugo
supporting information; experimental part, p. 6726 - 6728 (2010/03/25)
N6-(N'-Arylcarbamoyl)-2'-deoxyadenosine-H-phosphonates displayed molecular recognition towards cationic phenothiazinium and phenoxazinium dyes in aqueous solutions; studies have shown that binding is driven mainly by aromatic interactions and t
New thermolytic carbamoyl groups for the protection of nucleobases
Ohkubo, Akihiro,Kasuya, Rintaro,Miyata, Kenichi,Tsunoda, Hirosuke,Seio, Kohji,Sekine, Mitsuo
experimental part, p. 687 - 694 (2009/06/20)
It was found that N-arylcarbamoyl and N-(phenylsulfonyl)carbamoyl (psc) groups could be effectively introduced onto the amino groups of deoxycytidine and deoxyadenosine derivatives and could be removed thermolytically. We succeeded in synthesizing DNA pro
