906641-22-3

Upstream product

• 906641-13-2 (1R,5S,6R)-5,6-bis(benzyloxy)-4-oxocyclohex-2-en-1-yl benzoate 
• 906641-11-0 methyl 2-O-benzoyl-3,4-di-O-benzyl-6-deoxy-α-D-lyxo-hex-5-enopyranoside 
• 906641-10-9 methyl 2-O-benzoyl-3,4-di-O-benzyl-6-deoxy-6-iodo-α-D-mannopyranoside 
• 57783-73-0 methyl 3,4-di-O-benzyl-α-D-mannopyranoside 
• 906641-16-5 (1R,4S,5R,6R)-5,6-Bis-benzyloxy-4-(4-methoxy-benzyloxy)-cyclohex-2-enol 
• 906641-18-7 (1S,4R,5S,6R)-5,6-bis(benzyloxy)-4-[[tert-butyl(dimethyl)silyl]oxy]cyclohex-2-en-1-ol 
• 906641-09-6 (2S,3S,4R,5S,6S)-4,5-Bis-benzyloxy-6-iodomethyl-2-methoxy-tetrahydro-pyran-3-ol 
• 100-44-7 benzyl chloride 
• 906641-21-2 (1R,2R,3S,4R,5S,6R)-3,4-bis(benzyloxy)-2-[[tert-butyl(dimethyl)silyl]oxy]-6-(hydroxymethyl)-5-[(4-methoxybenzyl)oxy]cyclohexanol 
• 906641-20-1 [[(1R,2S,3S,4R,5R,6R)-3,4-bis(benzyloxy)-5-[(4-methoxybenzyl)oxy]-7-oxabicyclo[4.1.0]hept-2-yl]oxy](tert-butyl)dimethylsilane 
• 906641-17-6 [(1R,4S,5R,6S)-5,6-bis(benzyloxy)-4-[(4-methoxybenzyl)oxy]cyclohex-2-en-1-yl]oxy(tert-butyl)dimethylsilane 
• 906641-15-4 (1R,4S,5R,6R)-5,6-bis(benzyloxy)-4-[(4-vethoxybenzyl)oxy]cyclohex-2-en-1-yl benzoate 
• 906641-19-8 (1R,2R,3S,4S,5S,6R)-3,4-bis(benzyloxy)-5-[[tert-butyl(dimethyl)silyl]oxy]-7-oxabicyclo[4.1.0]heptan-2-ol 
• 906641-14-3 (1R,4S,5R,6R)-5,6-bis(benzyloxy)-4-hydroxycyclohex-2-en-1-yl benzoate 

Downstream Products

• 906641-23-4 (1S,2S,3R,4R,5R,6R)-2,3,4,5-tetrakis(benzyloxy)-6-[(benzyloxy)methyl]cyclohexyl methanesulfonate 
• 906748-03-6 (1S,2R,3S,4R,5R,6S)-2,3,4,5-tetrakis(benzyloxy)-6-[(benzyloxy)methyl]cyclohexanol 

Relevant academic research and scientific papers

Synthesis of cyclophellitol utilizing a palladium chloride mediated-ferrier-II rearrangement

Cyclophellitol and its C3-epimer have been synthesized from 5-enoglucopyranoside and 5-enomannopyranoside, respectively. The carbocyclic skeleton was constructed through a Ferrier-II reaction meditated by PdCl 2.