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Upstream product

• 434-45-7 2,2,2-Trifluoroacetophenone 
• 343338-28-3 (S)-2-methylpropane-2-sulfinamide 

Downstream Products

• 1269535-38-7 (S)-N-((R)-1,1,1-trifluoro-2-phenyldec-3-yn-2-yl)-2-methylprop-2-ylsulfinamide 
• 1269535-40-1 (S)-N-((R)-1,1,1,5,5,5-hexafluoro-2-phenylpent-3-yn-2-yl)-2-methylprop-2-ylsulfinamide 
• 1269535-54-7 (R)-4-cyclopropyl-1,1,1-trifluoro-2-phenylbut-3-yn-2-amine 
• 1269535-37-6 (S)-N-((R)-4-cyclopropyl-1,1,1-trifluoro-2-phenylbut-3-yn-2-yl)-2-methylprop-2-ylsulfinamide 
• 1269535-36-5 (S)-N-((R)-1,1,1-trifluoro-2,4-diphenylbut-3-yn-2-yl)-2-methylprop-2-ylsulfinamide 
• 1269535-39-8 (S)-N-((R)-1,1,1-trifluoro-2-phenyloct-3-yn-2-yl)-2-methylprop-2-ylsulfinamide 
• 1269535-59-2 (S)-N-((S)-1,1,1-trifluoro-2-phenylbut-3-yn-2-yl)-2-methylprop-2-ylsulfinamide 
• 1269535-41-2 (S)-N-((R)-1,1,1-trifluoro-2-phenyl-4-(trimethylsilyl)but-3-yn-2-yl)-2-methylprop-2-ylsulfinamide 
• 1472660-67-5 dimethyl (S)-2-((S)-1,1-dimethylethyl sulfinamido)-3,3,3-trifluoro-2-phenylpropylphosphonate 
• 1381765-59-8 (S)-2-methyl-N-((R)-1,1,1-trifluoro-4-oxo-2-phenyl-4-o-tolylbutan-2-yl)propane-2-sulfinamide 
• 1381765-58-7 (S)-2-methyl-N-((S)-1,1,1-trifluoro-4-oxo-2-phenyl-4-o-tolylbutan-2-yl)propane-2-sulfinamide 
• 1381765-57-6 (S)-2-methyl-N-((S)-1,1,1-trifluoro-4-(4-methoxyphenyl)-4-oxo-2-phenylbutan-2-yl)propane-2-sulfinamide 
• 1381765-54-3 (S)-2-methyl-N-((R)-1,1,1-trifluoro-4-oxo-2-phenyl-4-p-tolylbutan-2-yl)propane-2-sulfinamide 
• 1381765-53-2 (S)-2-methyl-N-((S)-1,1,1-trifluoro-4-oxo-2-phenyl-4-p-tolylbutan-2-yl)propane-2-sulfinamide 

Relevant academic research and scientific papers

A general and highly selective method for the asymmetric synthesis of trifluoromethyl-substituted α- And β-aminophosphonates

A highly selective method for the asymmetric formation of trifluoromethyl-substituted α- and β-aminophosphonates was described. The reaction proceeded with high yields and good to excellent diastereoselectivity. The product can be easily converted into corresponding trifluoromethyl-substituted aminophosphoric acids. A highly selective method for the asymmetric formation of trifluoromethyl-substituted α- and β-aminophosphonates was described. The reaction proceeded with high yields and good to excellent diastereoselectivity. The product can be easily converted into corresponding trifluoromethyl-substituted aminophosphoric acids. Copyright

Highly diastereoselective synthesis of α-trifluoromethylated α-propargylamines by acetylide addition to chiral CF3- substituted N-tert-butanesulfinyl ketimines

A convenient and practical method for the preparation of enantiomerically pure α-trifluoromethylated α-propargylamines is described. A range of enantiopure α-trifluoromethylated α-propargyl sulfinamides were obtained by the addition of lithium acetylides