1277172-58-3

Upstream product

• 108275-52-1 (+)-(3S,4R)-3-benzyloxy-4,5-O-isopropylidene-4,5-dihydroxy-1-pentene 
• 76-83-5 trityl chloride 
• 115586-67-9 (2R,3S)-3-O-benzyl-4-pentene-1,2,3-triol 
• 100-39-0 benzyl bromide 
• 18524-19-1 (S)-1-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-prop-2-en-1-ol 

Downstream Products

• 1277172-59-4 (2R,3S)-3-(benzyloxy)-1-(trityloxy)pent-4-en-2-yl methanesulfonate 
• 1277172-80-1 (6R,7R,8R,8aS)-6,7,8-tris(benzyloxy)hexahydroindolizin-3(5H)-one 
• 1277172-81-2 (6R,7R,8R,8aR)-6,7,8-tris(benzyloxy)hexahydroindolizin-3(5H)-one 
• 1277172-79-8 benzyl (2S,3R,4R,5R)-3,4,5-tris(benzyloxy)-2-[(E/Z)-3-ethoxy-3-oxoprop-1-enyl]piperidine-1-carboxylate 
• 1277172-78-7 benzyl (2S,3R,4R,5R)-3,4,5-tris(benzyloxy)-2-(hydroxymethyl)piperidine-1-carboxylate 
• 1277172-76-5 benzyl (2S,3R,4R,5R)-3,4,5-tris(benzyloxy)-2-(trityloxymethyl)piperidine-1-carboxylate 
• 1277172-75-4 C₄₄H₄₃NO₈ 
• 1277172-74-3 benzyl (2S,3R,4R,5R)-3-(benzyloxy)-4,5-dihydroxy-2-(trityloxymethyl)piperidine-1-carboxylate 
• 1277172-73-2 benzyl (2S,3S)-3-(benzyloxy)-2-(trityloxymethyl)-1,2,3,6-tetrahydropyridine-1-carboxylate 
• 1277172-72-1 benzyl allyl[(2S,3S)-3-(benzyloxy)-1-(trityloxy)pent-4-en-2-yl]carbamate 
• 1277172-83-4 benzyl (2S,3S)-[3-(benzyloxy)-1-(trityloxy)pent-4-en-2-yl]carbamate 
• 1277172-70-9 (1R,2R,3R,4S,5R)-3-(benzyloxy)-4-(tert-butoxycarbonylamino)cyclohexane-1,2,5-triyl triacetate 
• 1277172-69-6 (1R,2R,3R,4S,5R)-5-(acetoxy)-3-(benzyloxy)-4-(tert-butoxycarbonylamino)cyclohexane-1,2-diol 
• 1277172-68-5 (3S,4S,5R)-5-(acetoxy)-3-(benzyloxy)-4-(tert-butoxycarbonylamino)cyclohex-1-ene 

Relevant academic research and scientific papers

Synthesis of aminocyclitols and trihydroxylated indolizidinone from a D-mannitol-derived common building block

The synthesis of 4-amino-4-deoxy-muco-quercitol (22), 4-amino-4-deoxy-(-)- vibo-quercitol (27) and also a trihydroxylated indolizidinone 38 from D-mannitol is described using ring-closing metathesis and diastereoselective dihydroxylation as the key steps.