170112-35-3Relevant academic research and scientific papers
Synthesis and NMR spectra of some new carbohydrate modified uridine phosphoramidites
Serafinowski, Pawel J.,Barnes, Colin L.
, p. 1529 - 1532 (2007/10/03)
The one step reaction of 2'- and 3'-keto derivatives of uridine with bromodifluoromethyl[tris(dimethylamino)]phosphonium bromide and zinc gives the corresponding 2'- and 3'-difluoromethylene nucleosides in good yield. Desilylation and phosphitylation of the resultant 2'- or 3'-hydroxyls provides the target 2'- and 3'-phosphoramidites 7 and 8 for use in oligonucleotide synthesis.
New method for the preparation of 3'- and 2'-phosphoramidites of 2'- and 3'-difluoromethyleneuridine
Serafinowski,Barnes
, p. 7929 - 7938 (2007/10/03)
The one step reaction of 2'- and 3'-keto derivatives of uridine 2a, 2b, 7a and 7b with bromodifluoromethyl[tris(dimethylamino)]phosphonium bromide (13) and zinc gives the corresponding 2'- and 3'-difluoromethylene nucleosides 3a, 3b, 8a and 8b in good yield. Removal of the silyl groups affords difluoromethylenated uridines 4a, 4b, 9a and 9b. Phosphitylation of 4a and 9a provides the target 2'- and 3'-phosphoramidites 5 and 10 for use in oligonucleotide synthesis.
