143135-23-3

Upstream product

• 75-16-1 methylmagnesium bromide 
• 143135-21-1 (1R,3S,5R,6R,8R,9R)-6-Hydroxy-11,11-dimethyl-5-<2-(tert-butyldiphenylsilyloxy)ethyl>-2,10,12-trioxatricyclo<7.3.0.0^3,8>dodecan-4-one 
• 143135-20-0 {(3aR,5S,6S,6aR)-5-[4-(tert-Butyl-diphenyl-silanyloxy)-butyryl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl}-acetaldehyde 
• 143135-14-2 3-C-<(2-Benzyloxy)ethyl>-3,6,7-trideoxy-1,2-O-isopropylidene-8-O-(tert-butyldiphenylsilyl)-α-D-allo/β-L-talo-octofuranose 
• 143135-15-3 3,6,7-Trideoxy-3-C-(2-hydroxyethyl)-1,2-O-isopropylidene-8-O-(tert-butyldiphenylsilyl)-α-D-allo/β-L-talo-octofuranose 
• 113918-88-0 (R)-1-{(3aR,5S,6R,6aR)-6-[2-(benzyloxy)ethyl]-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl}ethane-1,2-diol 
• 143135-45-9 (3aR,5S,6R,6aR)-6-(2-Benzyloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole-5-carbaldehyde 
• 113918-87-9 (3aR,5S,6R,6aR)-6-[2-(benzyloxy)ethyl]-2,2-dimethyl-5-[(R)-2,2-dimethyl-1,3-dioxolan-4-yl]tetrahydrofuro[2,3-d][1,3]dioxole 
• 18427-19-5 1,2;5,6-di-O-isopropylidene-3-(2-hydroxyethyl)-α-D-allofuranoside 
• 143135-46-0 1-[(3aR,5S,6R,6aR)-6-(2-Benzyloxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-butane-1,4-diol 
• 143135-13-1 3-C-<(2-Benzyloxy)ethyl>-3,6-dideoxy-1,2-O-isopropylidene-6-C-vinyl-α-D-allo/β-L-talofuranose 

Downstream Products

• 143135-36-8 (1R,3R,4S,5S,6S,8R,9R)-6-Hydroxy-4,11,11-trimethyl-5-<2-(tert-butyldiphenylsilyloxy)ethyl>-2,10,12-trioxatricyclo<7.3.0.0^3,8>dodecane 6-acetate 
• 143169-71-5 (1R,3R,4S,5R,6S,8R,9R)-6-Hydroxy-4,11,11-trimethyl-5-<2-(tert-butyldiphenylsilyloxy)ethyl>-2,10,12-trioxatricyclo<7.3.0.0^3,8>dodecane 6-acetate 
• 143169-67-9 (3aR,4aR,5S,6R,8aR,8bR)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-hexahydro-benzo[4,5]furo[2,3-d][1,3]dioxol-7-one 
• 143169-68-0 (3aR,4aR,5S,6S,8aR,8bR)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-hexahydro-benzo[4,5]furo[2,3-d][1,3]dioxol-7-one 
• 143169-66-8 (1R,3R,4S,5R,6S,8R,9R)-6-Hydroxy-4,11,11-trimethyl-5-<2-(tert-butyldiphenylsilyloxy)ethyl>-2,10,12-trioxatricyclo<7.3.0.0^3,8>dodecane 
• 143135-35-7 (1R,3R,4S,5S,6S,8R,9R)-6-Hydroxy-4,11,11-trimethyl-5-<2-(tert-butyldiphenylsilyloxy)ethyl>-2,10,12-trioxatricyclo<7.3.0.0^3,8>dodecane 
• 143135-25-5 (1R,3S,8R,9R)-4,11,11-Trimethyl-5-<2-(tert-butyldiphenylsilyloxy)ethyl>-2,10,12-trioxatricyclo<7.3.0.0^3,8>dodec-4-en-6-one 

Relevant academic research and scientific papers

Intramolecular aldol condensation applied to D-glucose-derived δ-ketoaldehydes: Access to enantiomerically pure six-membered carbocycles

An enantiomerically pure δ-ketoaldehyde 10, efficiently prepared from D-glucose, was subjected to an intramolecular aldol condensation. By using DBU as a base, the expecting aldol reaction took place smoothly giving the aldol 11 stereoselectively. Further