199184-05-9Relevant academic research and scientific papers
Chiral synthons for CARBA-β-D-ribonucleosides. Synthesis of CARBA-4- deoxypyrazofurin and isomeric CARBA-4-deaza-oxoformycin analogues
Mohar, Barbara,Kobe, Joze
, p. 443 - 456 (2007/10/03)
Multi-step transformation of enantiomerically pure synthons, (1S,2S,3R,4R)-(4-hydroxymethyl-2,3-isopropylidenedioxy-1-cyclopentyl) methyl butyrate {(-)-5} and (1R,5R,6R,7S)-6,7-(isopropylidenedioxy)-3- oxabicyclo[3.2.1]octane-2-one {(+)-11} into carba-4-deoxypyrazofurin 1 and isomeric carba-4-deaza-oxoformycin 2 analogues is presented.
The synthesis of enantiomerically pure pyrazolo[4,3-C]pyridine carbaribo C-nucleoside
Mohar, Barbara,Kobe, Joze
, p. 1427 - 1429 (2007/10/03)
The synthesis of (-)-3-[(1S,2S,3R,4R)-2,3-dihydroxy-4-(hydroxymethyl) cyclopentan-1-yl]-1H-pyrazolo[4,3-c]pyridine-4,6(5H,7H)-dione 3 was accomplished via enantiomerically pure carbocyclic 5-(β-D- ribofuranosyl)tetrazole 4.
