245054-33-5

Upstream product

• 98-88-4 benzoyl chloride 
• 245054-32-4 methyl (3R,4S,5R)-3-hydroxy-4,5-<(2S,3S)-2,3-dimethoxybutan-2,3-dioxy>-cyclohex-1-en-1-carboxylate 
• 65-85-0 benzoic acid 
• 245054-31-3 (2S,3S,4aR,8S,8aR)-methyl 8-hydroxy-2,3-dimethoxy-2,3-dimethyl-2,3,4a,5,8,8a-hexahydrobenzo[b][1,4]dioxine-6-carboxylate 
• 40983-58-2 methyl shikimate 
• 176798-26-8 (2S,3S,4aR,6S,8R,8aR)-6,8-Dihydroxy-2,3-dimethoxy-2,3-dimethyl-octahydro-benzo[1,4]dioxine-6-carboxylic acid methyl ester 
• 245054-30-2 methyl (4S,5R)-4,5-<(2S,3S)-2,3-dimethoxybutan-2,3-dioxy>-3-oxo-cyclohex-1-en-1-carboxylate 
• 183474-88-6 methyl (1S,4S,5R)-1-hydroxy-4,5-<(2S,3S)-2,3-dimethoxybutan-2,3-dioxy>-3-oxo-cyclohexan-1-carboxylate 

Downstream Products

• 40983-58-2 methyl shikimate 
• 245054-34-6 methyl (3R,4S,5R)-3-benzoyloxy-4,5-dihydroxy-cyclohex-1-en-1-carboxylate 

Relevant academic research and scientific papers

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

An efficient transformation of quinic acid to shikimic acid derivatives

The synthesis of (-)-methyl shikimate and (-)-methyl 3-epi-shikimate and the 3-aminoshikimate derivative have been achieved via short and efficient mutes from quinic acid.