133048-89-2Relevant articles and documents
Deoxygenation at the C3 position of d- and l-arabinofuranose: Stereospecific access to enantiomeric cordycepose derivatives
Da Paix?o Soares, Fábio,Silva, Maria Joselice E,Doboszewski, Bogdan
, p. 143 - 148 (2013/10/01)
Efficient synthesis of 3-deoxy-1,2-O-isopropylidene-β-d- and β-l-threo-pentofuranose (1,2-O-isopropylidene-β-d- and β-l-cordycepose) was accomplished starting from d- and l-arabinofuranose derivatives, respectively, by the action of LiBH(Et)3 on corresponding intermediate 3-O-lyxofuranosyl trifluoromethanesulfonates.
Elucidation of the 2-C-methyl-D-erythritol 4-phosphate pathway for isoprenoid biosynthesis: Straightforward syntheses of enantiopure 1-deoxy-D-xylulose from pentose derivatives
Hoeffler, Jean-Fran?ois,Grosdemange-Billiard, Catherine,Rohmer, Michel
, p. 3065 - 3067 (2007/10/03)
Optically pure 1-deoxy-D-xylulose, a key metabolite for feeding experiments in the methylerythritol phosphate pathway for isoprenoid biosynthesis, is conveniently synthesised from 1,2-O-isopropylidene-α-D-xylofuranose or from D-arabinose. This renders lab