145105-08-4

Upstream product

• 22328-43-4 2,5-dimethylbenzoyl chloride 
• 63126-47-6 (2S)-2-(methoxymethyl)-1-pyrrolidine 

Downstream Products

• 145105-10-8 ((S)-2-Methoxymethyl-pyrrolidin-1-yl)-((S)-1,2,5-trimethyl-cyclohexa-2,5-dienyl)-methanone 
• 145105-12-0 (S)-4-((S)-2-Methoxymethyl-pyrrolidine-1-carbonyl)-2,4,5-trimethyl-cyclohexa-2,5-dienone 
• 145105-23-3 (2S,4S,5R)-4-((S)-2-Methoxymethyl-pyrrolidine-1-carbonyl)-2,4,5-trimethyl-cyclohexanone 
• 145105-21-1 (2R,4S,5R)-4-((S)-2-Methoxymethyl-pyrrolidine-1-carbonyl)-2,4,5-trimethyl-cyclohexanone 
• 145105-14-2 (2S,4S,5S)-4-((S)-2-Methoxymethyl-pyrrolidine-1-carbonyl)-2,4,5-trimethyl-cyclohexanone 

Relevant academic research and scientific papers

Asymmetric syntheses of α,α,γ-trisubstituted-γ-butyrolactones and 2,2,3-trisubstituted glutaric acid derivatives from chiral benzamides

The enantioselective conversion of aromatic carboxylic acids to acyclic structural units containing three stereogenic centers is described.