143169-67-9

Upstream product

• 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 
• 143135-27-7 3-Deoxy-3-C-<2-hydroxy-5-<(tert-butyldiphenylsilyl)oxy>pentyl>-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 143135-33-5 3,6-Dideoxy-1,2-O-isopropylidene-3-C-<2-oxo-5-<(tert-butyldiphenylsilyl)oxy>pentyl>-α-D-allofuran-5-ulose 
• 143135-24-4 (3aR,4aS,5R,6S,8aR,8bR)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-hydroxy-2,2,5-trimethyl-hexahydro-benzo[4,5]furo[2,3-d][1,3]dioxol-7-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 
• 143135-21-1 (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 
• 143135-32-4 3-Deoxy-3-C-<2-hydroxy-5-<(tert-butyldiphenylsilyl)oxy>pentyl>-1,2-O-isopropylidene-α-D-allofuranose 
• 143135-23-3 (3aR,4aS,5R,6R,7R,8aR,8bR)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-octahydro-benzo[4,5]furo[2,3-d][1,3]dioxole-5,7-diol 
• 143135-42-6 (3aR,5S,6R,6aR)-6-[5-(tert-Butyl-diphenyl-silanyloxy)-2-hydroxy-pentyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole-5-carbaldehyde 
• 143135-40-4 5-(tert-Butyl-diphenyl-silanyloxy)-1-[(3aR,5S,6R,6aR)-5-(1-hydroxy-ethyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl]-pentan-2-ol 
• 143169-65-7 (3aR,4aS,5R,8aR,8bR)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,2,5-trimethyl-3a,4a,5,8,8a,8b-hexahydro-benzo[4,5]furo[2,3-d][1,3]dioxol-5-ol 
• 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 
• 143135-22-2 (1R,3S,8R,9R)-11,11-Dimethyl-5-<2-(tert-butyldiphenylsilyloxy)ethyl>-2,10,12-trioxatricyclo<7.3.0.0^3,8>dodec-5-en-4-one 
• 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 

Downstream Products

• 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 
• 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 
• 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 

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