1021490-99-2

Upstream product

• 1021490-97-0 phenyl 2-O-benzoyl-3,4-di-O-benzyl-1-thio-α-L-idopyranoside 
• 75-65-0 tert-butyl alcohol 

Downstream Products

• 1021491-04-2 methyl [tert-butyl (2-O-benzoyl-3,4-di-O-benzyl-α-L-idopyranosyl)uronate]-(1->4)-3,6-di-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside 
• 1021491-05-3 methyl [tert-butyl (2-O-benzoyl-3,4-di-O-benzyl-α-L-idopyranosyl)uronate]-(1->4)-3-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-6-O-(4-methoxy)phenyl-α-D-glucopyranoside 
• 1075217-45-6 methyl (tert-butyl 2-O-benzoyl-3,4-di-O-benzyl-α-L-idopyranosyluronate)-(1->4)-[2-azido-3-O-benzyl-2-deoxy-6-O-(4-methoxyphenyl)-α-D-glucopyranosyl]-(1->4)-(tert-butyl 2-O-benzoyl-3-O-benzyl-α-L-idopyranosideuronate) 

Relevant academic research and scientific papers

An efficient synthesis of l-idose and l-iduronic acid thioglycosides and their use for the synthesis of heparin oligosaccharides

Efficient preparations of thioglycoside derivatives of l-idose and l-iduronic acid are described. The method avoids the tedious chromatographic separations of furanose and pyranose anomeric mixtures, and affords the thioglycosides in a stereoselective man