110418-33-2

Upstream product

• 121408-73-9 Methyl 2-O-acetyl-5-O-benzyl-3,6-dideoxy-3-C-methyl-β-L-galactofuranoside 
• 110418-34-3 Methyl 5-O-benzyl-3,6-dideoxy-3-C-methyl-β-L-talofuranoside 
• 121408-75-1 Methanesulfonic acid (2S,3R,4R,5S)-5-((S)-1-benzyloxy-ethyl)-2-methoxy-4-methyl-tetrahydro-furan-3-yl ester 
• 121408-72-8 Trifluoro-methanesulfonic acid (2S,3R,4R,5S)-5-((S)-1-benzyloxy-ethyl)-2-methoxy-4-methyl-tetrahydro-furan-3-yl ester 
• 67-56-1 methanol 
• 110418-31-0 (1R,2S,3R,4R,5S)-5-Benzyloxy-1,2-epoxy-4-hydroxy-3-methylhexyl N,N-diisopropylcarbamate 
• 81445-44-5 (S)-2-(benzyloxy)propanal 
• 54783-72-1 ethyl (S)-2-(benzyloxy)propionate 
• 121408-73-9 Methyl 2-O-acetyl-5-O-benzyl-3,6-dideoxy-3-C-methyl-α-L-altrofuranoside 
• 121408-75-1 Methanesulfonic acid (2R,3S,4S,5R)-5-((S)-1-benzyloxy-ethyl)-2-methoxy-4-methyl-tetrahydro-furan-3-yl ester 
• 121408-72-8 Trifluoro-methanesulfonic acid (2R,3S,4S,5R)-5-((S)-1-benzyloxy-ethyl)-2-methoxy-4-methyl-tetrahydro-furan-3-yl ester 

Downstream Products

• 121408-78-4 Methyl 5-O-benzyl-3,6-dideoxy-2-O,3-C-dimethyl-β-L-galactofuranoside 
• 121408-72-8 Trifluoro-methanesulfonic acid (2R,3S,4S,5R)-5-((S)-1-benzyloxy-ethyl)-2-methoxy-4-methyl-tetrahydro-furan-3-yl ester 
• 121408-75-1 Methanesulfonic acid (2R,3S,4S,5R)-5-((S)-1-benzyloxy-ethyl)-2-methoxy-4-methyl-tetrahydro-furan-3-yl ester 
• 121408-87-5 5-O-Benzyl-3,6-dideoxy-3-C-methyl-L-altrofuranose 
• 121408-74-0 2-((S)-1-Benzyloxy-ethyl)-3-methyl-furan 
• 110418-33-2 Methyl 5-O-benzyl-3,6-dideoxy-3-C-methyl-α-L-altrofuranoside 
• 121408-73-9 Methyl 2-O-acetyl-5-O-benzyl-3,6-dideoxy-3-C-methyl-α-L-altrofuranoside 

Relevant academic research and scientific papers

Enantiomerically Pure 2-(Carbamoyloxy)oxiranes and Their Utility in the Synthesis od D- and L-3,6-Dideoxy-3-C-methylhexofuranosides via the Homoaldol Reaction

As an example of a novel flexible strategy in the rapid enantioselective construction of branched carbohydrate analogues by the homoaldol reaction, the title compounds were synthesized. α-Metalated (E)-2-butenyl N,N-diisopropylcarbamate is added to (S)- or (R)-2-benzyloxypropanal.The homoaldol adducts are epoxidized; methanolysis affords furanosides of branched 3,6-dideoxyaldohexoses, or, hydrolysis yields the furanoses.