33302-99-7Relevant articles and documents
Synthesis of 4-deoxy and 4-deoxy-4-halogeno derivatives of L-fucose as potential enzyme inhibitors
Lindhorst, Thisbe K.,Thiem, Joachim
, p. 119 - 129 (2007/10/02)
Methyl-2,3-di-O-benzoyl-6-deoxy-α-L-galactopyranoside (2) was converted into the 4-deoxy-4-iodo-α-L-gluco derivative 4 by triflate-mediated inversion.Catalytic reduction of 4 gave methyl 2,3-di-O-benzoyl-4,6-dideoxy-α-L-xylo-hexopyranoside (6) and subsequ
Formal total synthesis of grahamimycin A1
Ohta,Mitsunobu
, p. 517 - 520 (2007/10/02)
(S)-t-Butyldimethylsiloxy-2-hexenoic acid and its (R)-isomer were prepared from (S)- and (R)-3-hydroxybutanoic acid esters, respectively. Condensation of the both isomers with 2-(p-toluenesulfonyl)ethyl (4S,5S,7R)-7-hydroxy-4,5-dimethylmethylenedioxyoctan
SYNTHESIS OF 4,6-DIDEOXY-D- AND -L-HEXOSES FROM RACEMIC AND meso-DIPROPENYLGLYCOL
Kuefner, Ulrike,Schmidt, Richard R.
, p. 211 - 224 (2007/10/02)
Rac- and meso-divinylglycols offer, via site-selective epoxidation, a versatile strategy for the synthesis of optically pure sugars.This is exemplified in this paper by the synthesis of 4,6-dideoxyhexoses.Starting from mono-O-benzyl di-(1-propenyl)glycol,