112929-26-7

Upstream product

• 84366-59-6 (2S,3R,4R)-2,3,5-tri-O-benzyl-pentane-1,4-diol 
• 14131-62-5 D-glucosamine hydrochloride 
• 104655-87-0 3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-α-D-glucopyranosyl bromide 
• 112929-24-5 1,3,4,6-tetra-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-α-D-glucopyranose 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 146934-02-3 2-deoxy-2-(allyloxycarbonylamino)-α-D-glucopyranoside 
• 112929-24-5 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(allyloxycarbonylamino)-β-D-glucopyranose 
• 112929-28-9 2,3,5-tri-O-benzyl-1-O-tertiobutyldimethylsilyl-D-ribitol 

Relevant academic research and scientific papers

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