696574-71-7

Upstream product

• 40983-58-2 methyl shikimate 
• 696574-72-8 methyl (3R,4S,5R)-5-hydroxy-3,4-(2,3-dimethoxybutane-2,3-dioxy)-1-cyclohex-1-ene-1-carboxylate 
• 433693-06-2 methyl (3R,4S,5R)-3-[(tert-butyldimethylsilyl)oxy]-4,5-(2,3-dimethoxybutan-2,3-dioxy)cyclohex-1-ene-1-carboxylate 
• 245054-32-4 methyl (3R,4S,5R)-3-hydroxy-4,5-<(2S,3S)-2,3-dimethoxybutan-2,3-dioxy>-cyclohex-1-en-1-carboxylate 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 98-88-4 benzoyl chloride 
• 696574-73-9 (3R,4S,5R)-3-O-(tert-butyldimethylsilyl)-4,5-(2,3-dimethoxybutane-2,3-dioxy)-cyclohex-1-ene-1-methanol 

Downstream Products

• 696574-74-0 (1R,2R,3R,4S,5R)-1-benzoyloxymethyl-1,2-dihydroxy-3-O-(tert-butyldimethylsilyl)-4,5-(2,3-dimethoxybutane-2,3-dioxy)-cyclohexane 
• 696574-77-3 (1R,2R,3S)-1-benzoyloxymethyl-1,2-O,O-isopropylidene-3-hydroxy-cyclohex-4-ene 

Relevant academic research and scientific papers

Synthesis of (+)-zeylenone from shikimic acid

Starting from shikimic acid, the total synthesis of zeylenone was studied. The product was proved to be the (+)antipode of zeylenone through analysis and comparison of their respective spectra (including NMR, MS, IR and CD) and optical data. The absolute

A Lemieux-Johnson oxidation of shikimic acid derivatives: Facile entry to small library of protected (2S,3S,4R)-2,3,4,7-tetrahydroxy-6-oxoheptanals

The Lemieux-Johnson oxidation was employed for the cleavage of the carbon-carbon double bond of shikimic acid derivatives. Through this procedure, a series of the sixteen novel (2S,3S,4R)-2,3,4,7-tetrahydroxy-6-oxoheptanals bearing three contiguous stereo