112929-28-9

Upstream product

• 84366-59-6 (2S,3R,4R)-2,3,5-tri-O-benzyl-pentane-1,4-diol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 64363-77-5 methyl 2,3,5-tri-O-benzyl-D-ribofuranoside 
• 16838-89-4 2,3,5-tri-O-benzyl-D-ribofuranose 

Downstream Products

• 76548-23-7 tetrahydro-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[2,1-d]-1,3-oxazol-2-one 
• 112929-26-7 4-O-(3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-β-D-glucopyranosyl)-2,3,5-tri-O-benzyl-1-tertiobutyldimethylsilyl-D-ribitol 
• 291758-08-2 2,3,5-tri-O-benzyl-1-O-tert-butyldimethylsilyl-4-O-p-nitrobenzoyl-L-lyxitol 
• 291758-09-3 2,3,5-tri-O-benzyl-L-lyxitol 
• 291758-10-6 1,4-anhydro-2,3,5-tri-O-benzyl-4-thio-D-ribitol 
• 620960-74-9 (S)-2-[(2S,3R,4S)-5-Azido-2-[(S)-2-tert-butoxycarbonylamino-3-(4-hydroxy-3,5-diiodo-phenyl)-propionylamino]-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-pentanoylamino]-3-(3,5-dibromo-4-hydroxy-phenyl)-propionic acid methyl ester 
• 620960-73-8 (S)-2-{(2S,3R,4S)-5-Azido-2-[(S)-2-tert-butoxycarbonylamino-3-(4-hydroxy-3,5-diiodo-phenyl)-propionylamino]-3,4-dihydroxy-pentanoylamino}-3-(3,5-dibromo-4-hydroxy-phenyl)-propionic acid methyl ester 
• 620960-72-7 (S)-2-[(2S,3R,4S)-5-Azido-2-tert-butoxycarbonylamino-3,4-bis-(tert-butyl-dimethyl-silanyloxy)-pentanoylamino]-3-(3,5-dibromo-4-hydroxy-phenyl)-propionic acid methyl ester 
• 620960-69-2 4-(N-tert-butoxycarbonyl)amino-4-deoxy-2,3,5-tri-O-benzyl-1-O-tert-butyldimethylsilyl-D-ribitol 
• 620960-93-2 (S)-2-((2S,3R,4S)-5-Azido-2-tert-butoxycarbonylamino-3,4-dihydroxy-pentanoylamino)-3-(3,5-dibromo-4-hydroxy-phenyl)-propionic acid methyl ester 
• 620960-87-4 4-azido-4-deoxy-2,3,5-tri-O-benzyl-1-O-tert-butyldimethylsilyl-D-ribitol 
• 620960-68-1 (2S,3R,4S)-1,3,4-Tris-benzyloxy-5-(tert-butyl-dimethyl-silanyloxy)-pentan-2-ol 

Relevant academic research and scientific papers

The stereoselective synthesis of 4'-β-thioribonucleosides via the pummerer reaction

An efficient stereoselective synthesis of 4'-β-thioribonucleosides 14, 15, 27, and 30 using the Pummerer reaction as the key step is described. The Pummerer reaction of 1,4-anhydro-2-O-(2,4-dimethoxybenzoyl)-3,5-O-(1,1,3,3-tetraisopro pyldisiloxane-1,3-di

N-Allyloxycarbonyl derivatives of D-glucosamine as promotors of 1,2-trans-glucosylation in Koenigs-Knorr reactions and in Lewis acid catalysed condensations

The use of suitably blocked D-glucosamine derivatives possessing the N-allyloxyxarbonyl protective group of the amino function represents potential new routes to 1,2-trans-glucosylations.Both 3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-α-D-glu