69187-61-7

Upstream product

• 677-22-5 tert-butylmagnesium chloride 
• 622-29-7 N-Benzylidenemethylamine 
• 3376-23-6 N-methyl-α-phenylnitrone 
• 594-19-4 tert.-butyl lithium 
• 1822-73-7 phenylthioethylene 
• 42071-02-3 1-Phenyl-1-formylamin-2,2-dimethylpropan 
• 51029-13-1 N-benzyl-N-methyl triflamide 
• 938-16-9 2,2-dimethylpropiophenone 
• 61501-04-0 2,2-dimethyl-1-phenyl-propylamine 

Relevant academic research and scientific papers

Triflamides: Elimination of the triflyl anion versus substitution of the trifluoromethide group

Base-induced elimination of CF3SO2- and nucleophilic substitution of CF3- were observed in the reaction of secondary triflamides with alkyllithium reagents.

A New Synthesis of β-Phenylaminothioesters and β-Lactams Via Base-Induced Ring-Opening of 2-Phenyl-3-Aryl-5-Phenyl-Thioisoxazolidines

1,3-Dipolar cycloaddition of phenyl vinyl sulfide to aryl N-phenyl, N-methyl, or N-t-butylnitrones affords 2-phenyl(or 2-methyl or 2-t-butyl)-3-aryl-5-phenylthioisoxazolidines according to the regioselectivity already known for the cycloaddition of not hi