113965-64-3

Upstream product

• 383-63-1 ethyl trifluoroacetate, 
• 1519-39-7 (R)-methyl p-tolyl sulfoxide 

Downstream Products

• 113965-66-5 (2S,R_S)-1-(4-methylphenyl)sulfinyl-3,3,3-trifluoropropan-2-ol 
• 113965-65-4 (2R)-1,1,1-trifluoro-3(R)-<(4-methylphenyl)sulfinyl>propan-2-ol 
• 169137-94-4 (Z)-2-((R)-Toluene-4-sulfinyl)-1-trifluoromethyl-vinylamine 
• 169137-91-1 [(Z)-2-((R)-Toluene-4-sulfinyl)-1-trifluoromethyl-vinyl]-carbamic acid benzyl ester 
• 121898-26-8 (S)-2-Phenyl-propionic acid (R)-2,2,2-trifluoro-1-p-tolylsulfanylmethyl-ethyl ester 
• 121898-27-9 (R)-2-Phenyl-propionic acid (R)-2,2,2-trifluoro-1-p-tolylsulfanylmethyl-ethyl ester 
• 121898-19-9 (R)-1-2,2,2-Trifluoro-1-(p-tolylthiomethyl)ethyl hydrogen phthalate 
• 121898-14-4 (R)-1,1,1-Trifluoro-3-p-tolylsulfanyl-propan-2-ol 
• 177267-98-0 Allyl-[(Z)-2-((R)-toluene-4-sulfinyl)-1-trifluoromethyl-vinyl]-carbamic acid benzyl ester 
• 177268-09-6 (S)-2,2,2-Trifluoro-1-p-tolylsulfanylmethyl-ethylamine 
• 169138-02-7 [(S)-2,2,2-Trifluoro-1-((R)-toluene-4-sulfinylmethyl)-ethyl]-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Highly Stereoselective Asymmetric Michael Addition Reactions Employing (R;E)-3,3,3-Trifluoroprop-1-enyl p-Tolyl Sulphoxide

(R;E)-3,3,3-Trifluoroprop-1-enyl p-tolyl sulphoxide, prepared in three steps from ethyl trifluoroacetate, showed a high degree of diastereoselectivity in Michael addition reactions with enolates; by this means, optically active trifluoromethylated organic molecules can be obtained readily in high yield as well as in high optical purity.