151693-58-2

Upstream product

• 151693-57-1 (1R,2R,3S,4R,5R)-3,4-di-O-benzyl-5-benzyloxymethyl-1,2-O-cyclohexylidenecyclohexane-1,2,3,4-tetraol 
• 1151903-41-1 C₃₂H₄₀O₇ 
• 100-39-0 benzyl bromide 
• 135735-91-0 (1R,2R,3S,4R,5R)-3-O-Benzyl-5-benzyloxymethyl-1,2-O-cyclohexylidene-cyclohexan-1,2,3,4-tetraol 

Downstream Products

• 151765-54-7 (1S,2S,3R,4R,5R,6R)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)-7-oxabicyclo[4.1.0]heptan-2-ol 
• 151693-63-9 (1S,2R,3R,4R,5R,6R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-7-oxa-bicyclo[4.1.0]heptan-2-ol 
• 161596-07-2 (1R,2S,3R,4R,5R,6S)-3,4-Bis-benzyloxy-5-benzyloxymethyl-7-oxa-bicyclo[4.1.0]heptan-2-ol 
• 151765-52-5 (1R,2R,3R,4R,5R,6S)-3,4-Bis-benzyloxy-5-benzyloxymethyl-7-oxa-bicyclo[4.1.0]heptan-2-ol 
• 126661-83-4 cyclophellitol 
• 161596-09-4 (1R,2R,3S,4R,5R,6R)-3,4-di-O-benzyl-5-benzyloxymethyl-2-O-tert-butyldimethylsilyl-7-oxabicyclo<4.1.0>heptane-2,3,4-triol 
• 161484-60-2 (1S,2S,3R,4S)-2,3-di-O-benzyl-5-benzyloxymethyl-1-O-tert-butyldimethylsilylcyclohex-5-ene-1,2,3-triol 
• 161596-08-3 (1R,2S,3R,4S)-2,3-di-O-benzyl-4-benzyloxymethyl-1-(O-tert-butyldimethylsilyl)cyclohex-5-ene-1,2,3-triol 
• 161484-59-9 (1R,2R,3R,4S,6R)-3-O-acetyl-1,2-di-O-benzyl-6-benzyloxymethyl-4-iodocyclohexane-1,2,3-triol 
• 158182-10-6 (1R,2R,3R,4S,6R)-1,2-di-O-benzyl-6-benzyloxymethyl-4-iodocyclohexane-1,2,3-triol 
• 151693-65-1 (1R,2S,3S,4S,5R,6R)-3-O-acetyl-4,5-di-O-benzyl-6-benzyloxymethyl-1,2-epoxycyclohexane-3,4,5-triol 
• 151765-53-6 (1S,2R,3S,4S,5R,6R)-3-O-acetyl-4,5-di-O-benzyl-6-benzyloxymethyl-1,2-epoxycyclohexane-3,4,5-triol 
• 161596-05-0 (1S,2R,3R,4R)-2,3-di-O-benzyl-4-benzyloxymethylcyclohex-5-ene-1,2,3-triol 
• 161596-04-9 (1R,2R,3R,4R)-2,3-di-O-benzyl-4-benzyloxymethylcyclohex-5-ene-1,2,3-triol 

Relevant academic research and scientific papers

(-)-Quinic Acid in Organic Synthesis. Part 4. Syntheses of Cyclophellitol and its (1R,6S)-, (2S)-, (1R,2S,6S)-Diastereoisomers

Cyclophellitol 1 and its (1R,6S)-, (2S)-, (1R,2S,6S)-diastereoisomers 2, 3 and 4 are constructed from quinic acid involving the following key steps: regioselective cyclic sulfate ring opening, regiospecific oxidative elimination and an epoxidation.Diastereoisomers 1, 2, 3 and 4 are characterized as their corresponding tetraacetates 5, 6, 7 and 8.

Chemoenzymatic syntheses of carbasugar analogues of nucleoside diphosphate sugars: UDP-carba-Gal, UDP-carba-GlcNAc, UDP-carba-Glc, and GDP-carba-Man

Chemoenzymatic syntheses of several NDP-carba-sugars have been successfully carried out, and these essential cofactor analogues are expected to be selective inhibitors of glycosyltransferase enzymes. The Royal Society of Chemistry.