136171-89-6

Upstream product

• 17690-16-3 benzyl bromomethyl ether 
• 136029-21-5 (1S,2S,6S,7R,10R)-4,4,10-Trimethyl-3,5,8,11-tetraoxa-tricyclo[5.3.1.0^2,6]undecan-9-one 
• 118244-90-9 (1S,2S,6S,7R)-4,4-Dimethyl-3,5,8,11-tetraoxa-tricyclo[5.3.1.0^2,6]undecan-9-one 
• 127588-86-7 (1RS,4RS,5SR,6SR,7SR)-6-exo,7-exo-(isopropylidenedioxy)-4-exo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one 
• 84121-01-7 6-exo,7-exo-(isopropylidenedioxy)-2,8-dioxabicyclo<3.2.1>octan-3-one 

Downstream Products

• 136029-29-3 (R)-3-Benzyloxy-2-((3aS,4S,6S,6aS)-6-hydroxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-2-methyl-propionic acid methyl ester 
• 127588-96-9 (R)-4-Benzyloxy-3-((3aS,4S,6aS)-6-hydroxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-3-methyl-butan-2-one 
• 136029-31-7 -5-deoxy-2,3-O-isopropylidene-5-methyl-β-L-allo-hexofuranosid>uronic acid 
• 136029-34-0 methyl 6-O-benzyl-5-<<(benzyloxy)carbonyl>amino>-5-deoxy-2,3-O-isopropylidene-5-methyl-α-D-talo-hexofuranoside 
• 136029-32-8 C₂₂H₃₀O₉ 
• 136029-30-6 methyl -5-deoxy-2,3-O-isopropylidene-5-methyl-β-L-allo-hexofuranosid>uronate 
• 136029-30-6 methyl -5-deoxy-2,3-O-isopropylidene-5-methyl-α-L-allo-hexofuranosid>uronate 
• 139391-43-8 methyl 6-O-benzyl-5-deoxy-5-isocyanato-2,3-O-isopropylidene-5-methyl-α-D-talo-hexofuranoside 
• 127588-97-0 5-<(benzyloxy)methyl>-5,7-dideoxy-2,3-O-isopropylidene-5-C-methyl-αβ-L-allo-heptos-6-ulofuranosyl acetate 
• 127588-96-9 (R)-4-Benzyloxy-3-((3aS,4S,6aS)-6-hydroxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-3-methyl-butan-2-one 
• 136029-32-8 C₂₂H₃₀O₉ 
• 136029-34-0 (+/-)-methyl 6-O-benzyl-5-<<(benzyloxy)carbonyl>amino>-5-deoxy-2,3-O-isopropylidene-5-methyl-α-D-talo-hexofuranoside 
• 127588-97-0 (+/-)-5-<(benzyloxy)methyl>-5,7-dideoxy-2,3-O-isopropylidene-5-C-methyl-αβ-L-allo-heptos-6-ulofuranosyl acetate 
• 139391-43-8 (+/-)-methyl 6-O-benzyl-5-deoxy-5-isocyanato-2,3-O-isopropylidene-5-methyl-α-D-talo-hexofuranoside 

Relevant academic research and scientific papers

Total, asymmetric synthesis of hexoses and azasugars branched at C(5)

The Diels-Alder adduct (-)-5 (a "naked sugar") of furan to 1-cyanovinyl (1R′)-camphanate was converted into (+)-(1R,5S,6S,7S)-6-exo,7-exo-(isopropylidenedioxy)-2,8-dioxabicyclo[3.2.1] octan-3-one and into (+)-(1R,5S,6S,7S)-7-endo-(benzyloxy)-6-exo- {[(t-b

ASYMMETRIC TOTAL SYNTHESIS OF AZASUGARS BRANCHED AT C-5

The new azasugars (5-ammonio-1,5-N-anhydro-5,6-dideoxy-5-C-methyl-αβ-L-ribo-hexitol)-1-sulfonate and (5-ammonio-1,5-N-anhydro-5-deoxy-5-C-methyl-αβ-D-talo-hexitol)-1-sulfonate have been derived from (1S,2R,4S)-2-cyano-7-oxabicyclohept-5-en-2-yl (1R

The Stereoselective Methylations and Hydroxymethylations of 2,8-Dioxabicyclooctan-3-one Derivatives. Synthesis of Branched-chain Sugars

The stereoselective C(4) alkylations of 6-exo,7-exo-(isopropylidenedioxy)-2,8-dioxabicyclooctan-3-one with MeI and PhCH2OCH2Br are presented; the products so-obtained have been converted to partially protected 5,6-dideoxy-5-C-methyl-D,L-ribo-hexofu