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Molecules ; 24(4)2019 Feb 13.
Article in English | MEDLINE | ID: mdl-30781738

ABSTRACT

A P(V)-N activation method based on nucleoside phosphoropiperidate/DCI system has been developed for improved synthesis of diverse UDP-furanoses. The reaction conditions including temperature, amount of activator, and reaction time were optimized to alleviate the degradation of UDP-furanoses to cyclic phosphates. In addition, an efficient and facile phosphoramidite route was employed for the preparation of furanosyl-1-phosphates.


Subject(s)
Arabinose/analogs & derivatives , Imidazoles/chemistry , Imino Furanoses/chemical synthesis , Arabinose/chemical synthesis , Arabinose/chemistry , Imino Furanoses/chemistry , Nucleosides/chemistry , Phosphates/chemistry , Piperidines/chemistry , Uridine/chemistry
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