199800-56-1Relevant academic research and scientific papers
Phthaloyl strategy - A new approach towards oligodeoxyribonucleotide synthesis
Beier, Markus,Pfleiderer, Wolfgang
, p. 1621 - 1624 (1997)
A new rapid strategy for machine-aided oligodeoxyribonucleotide synthesis has been established utilizing phthaloyl groups for protection of the heterocyclic amino functions within the phosphoramidite approach. A large number of DNA-sequences has been synt
Synthesis and properties of DNA oligomers containing 2′- deoxynucleoside N-oxide derivatives
Tsunoda, Hirosuke,Ohkubo, Akihiro,Taguchi, Haruhiko,Seio, Kohji,Sekine, Mitsuo
, p. 1217 - 1224 (2008/04/12)
(Chemical Equation Presented) Cytosine and adenine N-oxide derivatives have long been known as products resulting from the oxidative damage of DNA by peroxides such as hydrogen peroxide. Although the synthesis and properties of 2′-deoxynucleoside N-oxide
Nucleotides: Part LXI: Phthaloyl strategy: A new concept of oligonucleotide synthesis
Beier, Markus,Pfleiderer, Wolfgang
, p. 633 - 644 (2007/10/03)
A new alternative strategy of oligonucleotide synthesis was developed by use of the phthaloyl protecting group for the exocyclic amino functions of the nucleobases (see 9-12). This approach combines the advantages of cheap and easily accessible monomeric building blocks (see 17- 20), standard machine-aided oligonucleotide synthesis, and a fast deprotection protocol which is orthogonal to the cleavage procedure from the solid support. The crude oligonucleotides show high purity and require, in general, no further chromatographic purification.
