128790-83-0Relevant academic research and scientific papers
Reaction of 2-deoxy-2-C-(3-bromoacetoxypropyl)-α-D-arabinofuranosides with oligonucleotide
Mori,Katoh,Takenaka,Tanaka,Kaji,Samejima,Mitsunobu
, p. 2081 - 2104 (2007/10/02)
Reaction of methyl 2-deoxy-2-C-(3-bromoacetoxypropyl)-α-D- arabinofuranosides, prepared from methyl 2,3-anhydro-α-D-ribofuranoside, with oligodeoxyribonucleotide (21mer) in acetonitrile-H2O (pH 7) and subsequent treatment with piperidine resulted in the cleavage of the nucleotide chain at the position G, A, and C.
Regioselective Introduction of Allylic Groups into the C-2 or C-3 Position of Furanoside Rings
Ohmori, Junya,Shiotani, Tohru,Mitsunobu, Oyo
, p. 303 - 306 (2007/10/02)
The reaction of α-anomers of methyl 2,3-anhydro-D-ribo- and D-allo-furanosides with allylic Grignard reagents predominantly gave the corresponding 2-deoxy-2-C-alkenylfuranosides.In contrast, their β-anomers selectively gave 3-C-alkenyl derivatives.Prepara
