112543-78-9Relevant articles and documents
Click azide-alkyne cycloaddition for the synthesis of D-(-)-1,4- disubstituted triazolo-carbanucleosides
Broggi, Julie,Kumamoto, Hiroki,Berteina-Raboin, Sabine,Nolan, Steven P.,Agrofoglio, Luigi A.
experimental part, p. 1880 - 1888 (2009/09/29)
A revisited and improved synthesis of an optically active azido-carbanucleoside is reported. This azido precursor is used in the successful and versatile synthesis of enantiomerically pure D-(-)-1,4- disubstiluted 1,2,3-lriazolo-carbanuclcosides via coppe
AN ALTERNATIVE SYNTHESIS OF (1R,2S,3R,4R)-2,3-DIHYDROXY-4-HYDROXYMETHYL-1-CYCLOPENTANAMINE, A SYNTHETIC INTERMEDIATE OF (-)-ARISTEROMYCIN
Tadano, Kin-ichi,Hoshino, Masahide,Ogawa, Seiichiro,Suami, Tetsuo
, p. 2741 - 2744 (2007/10/02)
The title compound, an enantiomerically pure carbocyclic portion of the antibiotic (-)-aristeromycin, has been synthesized from D-erythrose.The synthesis involves a transformation of the known carbocyclic analogue of β-L-arabinofuranose to the α-D-ribo fo