867150-83-2

Upstream product

• 31350-91-1 (R)-chloromethyl p-tolyl sulfoxide 
• 67-64-1 acetone 

Downstream Products

• 867150-95-6 tert-butyl 2-{1-[chloro(p-tolylsulfinyl)methyl]-1-methylethyl}hexanoate 
• 956904-50-0 tert-butyl 2-dibenzylamino-4-chloro-3,3-dimethyl-4-(p-tolylsulfinyl)butanoate 
• 867151-02-8 (R)-2-[1,1-Dimethyl-2-((S)-toluene-4-sulfinyl)-ethyl]-hexanoic acid tert-butyl ester 
• 867150-99-0 (R)-2-Ethyl-3,3-dimethyl-4-((S)-toluene-4-sulfinyl)-butyric acid tert-butyl ester 
• 867150-85-4 (R)-2,3,3-Trimethyl-4-((S)-toluene-4-sulfinyl)-butyric acid tert-butyl ester 
• 867150-87-6 (R)-2,3,3-Trimethyl-4-((S)-toluene-4-sulfinyl)-butyric acid 
• 867150-92-3 (R)-4-Chloro-2-ethyl-3,3-dimethyl-4-((R)-toluene-4-sulfinyl)-butyric acid tert-butyl ester 

Relevant academic research and scientific papers

An asymmetric synthesis of carboxylic acid derivatives, including lactic acid and α-amino acid derivatives, from optically active 1-chlorovinyl p-tolyl sulfoxides and ester lithium enolates with creation of chirality at the α-position

Treatment of optically active 1-chlorovinyl p-tolyl sulfoxides, which were synthesized from symmetrical ketones or methyl formate and (R)-(-)-chloromethyl p-tolyl sulfoxide in three steps, with lithium enolate of carboxylic acid tert-butyl esters gave opt