128745-48-2

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 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 
• 128745-46-0 2-amino-6-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-2-deoxy-α,β-D-allofuranose 
• 128745-44-8 allyl 2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-α-D-allopyranoside 
• 128745-45-9 1-propenyl 2-amino-4,6-O-benzylidene-2-N,3-O-carbonyl-2-deoxy-α-D-allopyranoside 
• 76581-86-7 2-amino-2-N,3-O-carbonyl-2-deoxy-α,β-D-allofuranose 
• 83663-03-0 benzyl ((2S,3R,4R,5S,6R)-2-(allyloxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)carbamate 
• 128745-47-1 2-amino-6-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-deoxy-D-allitol 

Downstream Products

• 128745-49-3 (4S,5S)-4-(tert-Butyl-diphenyl-silanyloxymethyl)-2-oxo-oxazolidine-5-carbaldehyde 
• 128745-53-9 <2(S),3(R),4Z>-2-amino-1-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-4-hexadecene-1,3-diol 
• 128745-50-6 <2(S),3(R),4E>-2-amino-1-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-4-hexadecene-1,3-diol 
• 123447-03-0 <2(S),3(R),4Z>-2-amino-1-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-4-ocatadecene-1,3-diol 
• 123447-09-6 <2(S),3(R),4E>-2-amino-1-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-4-octadecene-1,3-diol 
• 128745-54-0 <2(S),3(R),4Z>-2-amino-1-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-4-eicosene-1,3-diol 
• 128745-51-7 <2(S),3(R),4E>-2-amino-1-O-(tert-butyldiphenylsilyl)-2-N,3-O-carbonyl-4-eicosene-1,3-diol 

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.