4784-41-2Relevant articles and documents
Synthesis of α-2'-deoxynucleosides
Larsen,Abdel Aleem,Pedersen
, p. 1645 - 1646 (1995)
α-Thyimdine (4) was synthesized from thyimdine (1) in 3 steps in 36% overall yield without using chromatography and with the possibility of increasing the yield to 85% by reusing the remaining α,β-mixture. 1-(2-Deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofu
Investigation of Stereoselectivities in the Coupling Reactions of 1-O-Methyl-3,5-di-O-p-toluoyl-2-deoxyribofuranoside with Purines and Pyrimidines
Janardhanam, Selvasekaran,Nambiar, Krishnan P.
, p. 3657 - 3660 (2007/10/02)
Stereoselectivities in the coupling rection between 1-O-methyl-3,5-di-O-p-toluoyl-2-deoxyribofuranoside and suitably protected purine and pyrimidine derivatives have been examined in acetonitrile with varying equivalents of SnCl4.The best result in α-nucleoside formation was obtained when the coupling reaction was carried out in the presence of ten equivalents of SnCl4.
Novel DNA Analog for Potential Gene Regulating Agent. A Convenient Synthesis of α-Oligodeoxyribonucleotide Phosphorothioate Bearing 3'-Monophosphate
Shinozuka, Kazuo,Morita, Tsutomu,Hirota, Yoshiki,Sawai, Hiroaki
, p. 1941 - 1944 (2007/10/02)
α-2'-Deoxyoctathymydilic acid phosphorothioate analog bearing 3'-monophosphate was conveniently synthesized via phosphoramidite method using a riboadenosine attached Teflon-based solid support.The obtained oligomer exhibited enhanced stability toward the digestion by common nucleases.