943439-98-3

Upstream product

• 76-83-5 trityl chloride 
• 38257-94-2 4-[(triphenylmethyl)oxy]butanol 
• 32293-02-0 4-iodobutyl trityl ether 
• 1651-41-8 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecan-1-ol 
• 42028-44-4 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-undecan-1-al 

Downstream Products

• 943440-00-4 [8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,15-heptadecafluoropentadec-4(Z)-en-1-yl] 6-O-[3,4-di-O-benzyl-2-O-pivaloyl-β-D-glucopyranosyl]-3,4-di-O-benzyl-2-O-pivaloyl-β-D-glucopyranoside 
• 943439-99-4 [8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,15-heptadecafluoropentadec-4(Z)-en-1-yl] 3,4-di-O-benzyl-2-O-pivaloyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Oligosaccharide synthesis in microreactors

Described is the combination of microreactors and fluorous phase chemistry to assemble oligosaccharides. The synthesis of a β-(1→6) linked D-glucopyranoside homotetramer serves to illustrate this approach. Glycosylations employing a Fmoc-protected glucosy