72076-13-2Relevant articles and documents
Regioselective synthesis of new sucrose derivatives via 3-ketosucrose
Pietsch,Walter,Buchholz
, p. 183 - 194 (1994)
3-Ketosucrose (α-D-ribo-hexopyranosyl-3-ulose-β-D-fructofuranoside), obtained from sucrose via microbial oxidation with Agrobacterium tumefaciens, was shown to be an appropriate and versatile synthon for regioselective syntheses. Condensation with hydroxy
Enantiomerically Pure Building Blocks from Sugars, 10 2,3-Dihydropyranones with Contiguous Chiral Centers: Practical Routes for Their Aquisition and Evaluation of their Reaction Potential
Lichtenthaler, Frieder W.,Nishiyama, Shigeru,Weimer, Thomas
, p. 1163 - 1170 (2007/10/02)
A practical, large-scale adaptable four-step procedure has been developed for the conversion of D-glucose into pyranoid enediolone esters with (R,R)-configuration in contiguous chiral centers, involving hydrolysis of the readily accessible bis-acetonide o