146388-97-8

Upstream product

• 765319-28-6 (1S,6R)-6-benzoylcyclohex-3-ene-1-carboxylic acid 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 31139-02-3 (1R,6S)-6-methoxycarbonyl-3-cyclohexene-1-carboxylic acid 
• 98-80-6 phenylboronic acid 
• 935-79-5 cis-1,2,3,6-tetrahydrophthalic anhydride 
• 31211-31-1 racemic cis-6-benzoylcyclohex-3-enecarboxylic acid 
• 857682-04-3 (1S,6R)-6-benzoyl-1-[(4S)-4-isopropyl-1,3-thiazolidine-2-thion-3-yl]carbonylcyclohex-3-ene 

Downstream Products

• 765319-28-6 (1S,6R)-6-benzoylcyclohex-3-ene-1-carboxylic acid 

Relevant academic research and scientific papers

Asymmetric synthesis of cis-4a,5,8,8a-tetrahydrophthalazin-1(2H)-one derivatives based on organocatalytic alcoholysis of cyclic dicarboxylic anhydride

Asymmetric synthesis of optically active cis-4-phenyl-4a,5,8,8atetrahydrophthalazin-1(2H)-one and its N-alkylated derivatives based on an organocatalytic enantioselective alcoholysis of cyclic dicarboxylic anhydride was described.

Practical synthesis of chiral cis-cyclohex-4-ene-1,2-dicarboxylic acid derivatives by utilizing (4S)-isopropyl-1,3-thiazolidine-2-thione

Both enantiomers of chiral cis-cyclohex-4-ene-1,2-dicarboxylic acid derivatives were synthesized by optical resolution of the corresponding enantiomeric mixtures by utilizing (4S)-isopropyl-1,3-thiazolidine-2-thione followed by mild aminolysis, methanolys

Cyclohexene derivative and method of producing the same

Provided is a novel (1R, 2S)-1-acyl-2-carboxycyclohex-4-ene derivative represented by the following general formula [I], and its producing method, STR1 (where R1 represents a hydrogen atom, a lower alkyl group, or substituted or unsubstituted a