191538-44-0Relevant academic research and scientific papers
An efficient and highly stereoselective synthesis of nucleoside derivatives from furanoid 1,2-diols
Robles, Rafael,Rodriguez, Concepcion,Izquierdo, Isidoro,Plaza, Maria T.,Mota, Antonio
, p. 2959 - 2965 (1997)
Reaction between suitably protected furanoid glycals 1b-4b, readily obtained from furanoid 1,2-diols (1a-4a), and different silylated pyrimidine bases, gave the corresponding 3',5'- and 3',5',6'-O-protected 2'-deoxy-2'-iodo-β-D-xylo-pentofuranosyl 5-10 and β-D-gluco-hexofuranosyl 11 nucleosides, respectively. Compound 5 has been transformed into its 2'-deoxy 12 and 2',3'-anhydro 14 derivatives. The high stereoselectivity of the reaction is discussed.
Synthesis of furanose glycals from furanose 1,2-diols and their cyclic thiocarbonate esters
Robles Diaz, Rafael,Rodriguez Melgarejo, Conception,Izquierdo Cubero, Isidoro,Plaza Lopez-Espinosa, Maria T.
, p. 375 - 380 (2007/10/03)
Two new methods for the synthesis of furanoid glycals are described. Both procedures were shown to be faster and cheaper that those previously reported. Protected 1,2-dihydroxypento- and hexo-furanose derivatives with the D-xylo, D-gluco and D-ribo, D-all
