162934-29-4Relevant academic research and scientific papers
Synthesis of β configured 2',3'-unsaturated pentopyranosyl nucleosides
Doboszewski,Blaton,Herdewijn
, p. 1321 - 1324 (1995)
Coupling of 3,4-di-O-p-nitrobenzoyl-D-xylal, with heterocyclic bases in boiling DMF in the absence of externally added acid catalyst constitutes a convenient way to β configured 2',3'-unsaturated pentopyranosyl nucleosides. Formation of the 3'-substituted
Easy Synthesis and Different Conformational Behavior of Purine and Pyrimidine β-D-glycero-Pent-2'-enopyranosyl Nucleosides
Doboszewski, Bogdan,Blaton, Norbert,Herdewijn, Piet
, p. 7909 - 7919 (2007/10/03)
Condensation of 3,4-bis-O-(p-nitrobenzoyl)-D-xylal with purines and pyrimidines (A, C, 6-chloropurine, G, T, U) without externally added acid catalyst leads to the 2',3'-unsaturated pentopyranosyl nucleosides in preparatively acceptable yields of both β a
