128745-45-9

Upstream product

• 128745-43-7 allyl 4,6-O-benzylidene-2-benzyloxycarbonylamino-2-deoxy-α-D-allopyranoside 
• 128745-41-5 allyl 4,6-O-benzylidene-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside 
• 128745-42-6 allyl 4,6-O-benzylidene-2-benzyloxycarbonylamino-2-deoxy-α-D-ribo-hexapyranosid-3-ulose 
• 100-52-7 benzaldehyde 
• 83663-03-0 benzyl ((2S,3R,4R,5S,6R)-2-(allyloxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)carbamate 
• 128745-44-8 allyl 2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-α-D-allopyranoside 

Downstream Products

• 128745-48-2 2-amino-1,6-di-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-2-deoxy-D-allitol 
• 128745-46-0 2-amino-6-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-2-deoxy-α,β-D-allofuranose 
• 128745-47-1 2-amino-6-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-deoxy-D-allitol 

Relevant academic research and scientific papers

An efficient, stereoselective synthesis of 4-E- and 4-Z-D-erythro-sphingenine and related compounds from 2-amino-2-deoxy-D-glucose.

Efficient, stereoselective synthesis of 4-E- and 4-Z-D-erythro-sphingenines having C16, C18, and C20 carbon-chains was achieved in 13 steps, starting from allyl 2-benzyloxycarbonylamino-2-deoxy-alpha-D-glucopyranoside. 2-Amino-1,6-di-O-tert- butyldiphenylsilyl-2-N,3-O-carbonyl-2-deoxy-D -allitol was used as the key intermediate.