478487-98-8Relevant academic research and scientific papers
Synthesis and anti-HCV activity of 1-(1′,3′-O-anhydro-3′-C-methyl-β-d-psicofuranosyl)uracil
Komsta, Zofia,Mayes, Benjamin,Moussa, Adel,Shelbourne, Montserrat,Stewart, Alistair,Tyrrell, Andrew J.,Wallis, Laura L.,Weymouth-Wilson, Alexander C.,Yurek-George, Alexander
, p. 6216 - 6219 (2015/01/09)
Synthesis of a novel 1′,2′-oxetane-uridine bearing a 2′-C-methyl substituent, [1-(1′,3′-O-anhydro-3′-C-methyl-β-d-psicofuranosyl)uracil], is described. Key to its construction was the use of 6-O-(p-toluoyl)-1,2:3,4-di-O-isopropylidene-3-C-methyl-d-psicofu
Synthesis, physicochemical and biochemical studies of 1′,2′- oxetane constrained adenosine and guanosine modified oligonucleotides, and their comparison with those of the corresponding cytidine and thymidine analogues
Pradeepkumar, Pushpangadan I.,Cheruku, Pradeep,Plashkevych, Oleksandr,Acharya, Parag,Gohil, Suresh,Chattopadhyaya, Jyoti
, p. 11484 - 11499 (2007/10/03)
We have earlier reported the synthesis and antisense properties of the conformationally constrained oxetane-C and -T containing oligonucleotides, which have shown effective down-regulation of the proto-oncogene c-myb mRNA in the K562 human leukemia cells.
Synthesis of anhydro psicofuranosyl nucleosides
Roivainen, Jarkko,Veps?l?inen, Jouko,Azhayev, Alex,Mikhailopulo, Igor A.
, p. 6553 - 6555 (2007/10/03)
Methyl 1-O-mesyl-5-O-toluoyl-β-D-psicofuranoside (5) was synthesised from the known 1,3;4,5-di-O-isopropylidene-β-D-psicofuranose (1) as a key carbohydrate precursor for the preparation of anhydro psicofuranosyl nucleosides. Transformation of 5 into aceta
