501433-74-5

Upstream product

• 98167-08-9 (3R,4S,5R)-3,4,5-triacetoxycyclohex-1-ene-1-carboxylic acid 

Downstream Products

• 109220-92-0 ((3R)-3r,4c,5t-triacetoxy-cyclohex-1-enyl)-methanol 
• 108988-52-9 (3R)-3r,4c,5t-triacetoxy-cyclohex-1-enecarbaldehyde 
• 120174-75-6 ent-11,17β-dimethoxy-18α-((3S)-3r,4c,5t-triacetoxy-cyclohex-1-enecarbonyloxy)-15β-yohimban-16α-carboxylic acid methyl ester 
• 1228688-44-5 1-iodo-(3R,4S,5R)-3,4,5-triacetoxy-1-cyclohexene 
• 1228688-59-2 1-chloro-(3R,4S,5R)-3,4,5-triacetoxy-1-cyclohexene 
• 1228688-58-1 1-bromo-(3R,4S,5R)-3,4,5-triacetoxy-1-cyclohexene 
• 51051-18-4 (3R,4S,5R)-3,4,5-Triacetoxy-1-cyan-1-cyclohexen 
• 111497-79-1 (3R)-3r,4c,5t-triacetoxy-1-benzoyloxymethyl-cyclohexene 
• 109369-56-4 (3R)-3r,4c,5t-trihydroxy-cyclohex-1-enecarbaldehyde-(2,4-dinitro-phenylhydrazone) 
• 906366-69-6 (3R)-3r,4c,5t-trihydroxy-cyclohex-1-enecarbaldehyde 

Relevant academic research and scientific papers

New aspects of the Hunsdiecker-Barton halodecarboxylation-syntheses of phospha-shikimic acid and derivatives

We report an efficient synthetic approach to phospha-isosteres of important intermediates of the shikimic acid pathway by the application of the Hunsdiecker-Barton halodecarboxylation to cyclohexenylcarboxylic acids. As examples, phospha-shikimic acid, it