35 research outputs found
Réactivité du bromure de 5-thioxylopyranosyle et du 1,5-dithioxylopyranoside vis-à-vis d’anions thiolate
Chemoenzymatic synthesis of 5-thio-D-xylopyranose.
5-thio-D-xylopyranose, a synthon used for the preparation of drugs with antithrombotic activity, was synthesised by an enzymatic isomerisation from the corresponding ketose, 5-thio-D-xylulofuranose, with glucose isomerase. This compound was obtained by two different chemoenzymatic routes, the key step being the stereospecific formation of a C-C bond, catalysed by transketolase or fructose-1,6-bisphosphate aldolas
ChemInform Abstract: Chemistry of 4-Cyanophenyl 1,5-Dithio-β-D-xylopyranoside (Beciparcil). Part 3. Synthesis of the 3-Methyl Ether and 4-Deoxy Derivatives of 4-Cyanophenyl 1,5-Dithio-β-D-xylopyranoside (Beciparcil).
A new chemoenzymatic route to dihydroxyacetone phosphate from glycidol for the in situ aldolase-mediated synthesis of monosaccharides
An efficient chemoenzymatic route to dihydroxyacetone phosphate from glycidol for the in situ aldoalse-mediated synthesis of monosaccharides
We report a new two-step procedure that uses inexpensive rac-glycidol to obtain valuable dihydroxyacetone phosphate (DHAP), a building block for the synthesis of monosaccharide analogues
