0194124 - UOCHB-X 20010207 RIV CZ eng J - Článek v odborném periodiku
Hřebabecký, Hubert - Holý, Antonín
Synthesis of carba analogues of deoxy-4-.I.C./I.-(hydroxymethyl)hexopyranoses, intermediates in the synthesis of carbocyclic nucleosides.
Collection of Czechoslovak Chemical Communications. Roč. 66, č. 5 (2001), s. 785-798. ISSN 0010-0765
Výzkumný záměr: CEZ:AV0Z4055905
Klíčová slova: carbasugars
Kód oboru RIV: CC - Organická chemie
Impakt faktor: 0.778, rok: 2001

3-O-Benzyl-1,2-O-isopropylidene-ŕ-.I.D./I.-glucofuranose-5,6-O-sulfate was transformed to (1.I.R./I.,2.I.S./I.,4.I.R./I.)-5,5-bis(hydroxymethyl)cyclohexane-1,2,4-triol and 3-O-benzyl-5,6-dideoxy-6-iodo-1,2-O-isopropylidene-ŕ-.I.D-xylo./I.-hexofuranose was converted to (1.I.R./I.,3.I.R./I.)-4,4-bis(hydroxymethyl)cyclohexane-1,3-diol.
Trvalý link: http://hdl.handle.net/11104/0089815