108319-57-9Relevant academic research and scientific papers
Formation of aureolic acid oligodeoxy mono-, di-, and trisaccharides employing the dibromomethyl methyl ether reaction
Thiem, Joachim,Sch?ttmer, Bernhard
, p. 279 - 293 (2017/12/12)
2,3-Isopropylidene D-rhamnopyranoside 2 obtained from mannose was treated with dibromomethyl methyl ether to give 2,6-dideoxy-2-bromo-glucopyranosyl bromide 5. Correspondingly, the D-talo precursor 3 led to the epimeric galacto-pyranosyl bromide 4. Both g
NEUE SYNTHESEN VON AUREOLSAEURETRISACCHARIDEN
Thiem, Joachim,Gerken, Manfred,Schoettmer, Bernhard,Weigand, Joachim
, p. 327 - 342 (2007/10/02)
The silver trifluoromethylsulfonate-promoted condensation of 4-O-benzoyl-2-bromo-2,6-dideoxy-3-O-formyl-α-D-glucopyranosyl bromide (4) and benzyl 4-O-benzoyl-2-bromo-2,6-dideoxy-β-D-glucopyranoside (5) yielded a disaccharide, which, after ester cleavage,
