141276-80-4

Upstream product

• 141318-32-3 methyl (Z)-3-<(1'S,2'R,3'S,5'R)-5'-benzyloxy-3'-methoxymethoxy-2'-(triethylsilyloxy)cyclohexyl>propenoate 
• 141276-75-7 (1S,2R,3S,5R)-3-benzoyloxymethyl-5-benzyloxy-1-methoxymethoxy-2-(triethylsilyloxy)cyclohexane 
• 141276-74-6 6-O-benzoyl-1-O-benzyl-3-O-methoxymethyl-5a-carba-α-L-lyxo-hexopyranose 
• 141276-78-0 (1S,2R,3S,5R)-5-benzyloxy-3-<(Z)-3-hydroxyprop-1-enyl>-1-methoxymethoxy-2-(triethylsilyloxy)cyclohexane 
• 141276-76-8 (1S,3R,4S,5R)-5-benzyloxy-3-hydroxymethyl-1-methoxymethoxy-2-(triethylsilyloxy)cyclohexane 
• 141276-73-5 (1R,6S,8R,10S)-8-benzyloxy-10-methoxymethoxy-3,3-dimethyl-2,4-dioxabicyclo<4.4.0>decane 
• 141103-94-8 (4-Methyl-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl)-methanol 
• 100-39-0 benzyl bromide 
• 994-30-9 triethylsilyl chloride 
• 141276-79-1 (1S,2R,3S,5R)-5-benzyloxy-3-<(Z)-3-(tert-butyldimethylsilyloxy)prop-1-enyl>-1-methoxymethoxy-2-(triethylsilyloxy)cyclohexane 

Downstream Products

• 168703-18-2 (1S,2R,3R,5R)-3-<(1S,2R)-3-(tert-butyldimethylsilyloxy)-1,2-bis(methoxymethoxy)propyl>-1-(methoxymethoxy)-2-(triethylsilyloxy)cyclohexan-5-ol 
• 141276-83-7 (3S,4R,5R)-5-<(1S,2R)-3-(tert-butyldimethylsilyloxy)-1,2-bis(methoxymethoxy)propyl>-3-methoxymethoxy-4-triethylsilyloxy-1-cyclohexanone 
• 141276-85-9 (1S,2R,3R,5S)-3-<(1S,2R)-3-(tert-butyldimethylsilyloxy)-1,2-bis(methoxymethoxy)propyl>-1,5-bis(methoxymethoxy)-2-triethylsilyloxy-5-vinylcyclohexane 
• 141276-86-0 C₃₈H₅₀O₉ 
• 141318-36-7 (1S,2R,3R,5R)-3-<(1S,2R)-3-(tert-butyldimethylsilyloxy)-1,2-bis(methoxymethoxy)propyl>-1-methoxymethoxy-2-triethylsilyloxy-5-vinylcyclohexan-5-ol 
• 141276-84-8 (1S,2R,3R,5S)-3-<(1S,2R)-3-(tert-butyldimethylsilyloxy)-1,2-bis(methoxymethoxy)propyl>-1-methoxymethoxy-2-triethylsilyloxy-5-vinylcyclohexan-5-ol 

Relevant academic research and scientific papers

Synthesis of carbocyclic analogues of 3-deoxy-D-manno-2-octulosonic acid and N-acetylneuraminic acid

A carbocyclic analogue of N-acetylneuraminic acid was synthesised from the Diels-Alder endo-adduct of furan and acrylic acid, and its ammonium salt was subjected to bioassay. In addition, carbocyclic analogues of 3-deoxy-D-manno-2-octulosonic acid were synthesised in racemic form from the same synthetic intermediate.

Synthesis of a Carbocyclic Analogue of N-Acetylneuraminic Acid (Pseudo-N-acetylneuraminic Acid)

A carbocyclic analogue of N-acetylneuraminic acid was synthesized from the Diels-Alder endo-adduct of furan and acrylic acid, and its ammonium salt was subjected to biological assay.