1039136-54-3

Upstream product

• 2916-68-9 2-(Trimethylsilyl)ethanol 
• 201230-82-2 carbon monoxide 
• 134481-27-9 N-(p-Anisyl)-2,2,2-trifluoroacetimidoyl iodide 
• 75999-66-5 (Z)-2,2,2-trifluoro-N-(4-methoxyphenyl)acetimidoyl chloride 

Downstream Products

• 1051442-81-9 2-(trimethylsilyl)ethyl 2-[(4-methoxyphenyl)(trimethylsilyl)amino]-2-(trifluoromethyl)-3-butenoate 
• 1039136-67-8 C₁₃H₁₄F₃NO₃ 
• 1039136-84-9 4-chlorobutyl (E)-3,3,3-trifluoro-2-(4-methoxyphenylimino)propanoate 
• 1039136-66-7 but-3-enyl (E)-3,3,3-trifluoro-2-(4-methoxyphenylimino)propanoate 
• 144008-26-4 3,3,3-Trifluoro-2-[(E)-4-methoxy-phenylimino]-propionic acid benzyl ester 
• 1039136-68-9 C₁₄H₁₆F₃NO₃ 
• 1039136-64-5 allyl (E)-3,3,3-trifluoro-2-(4-methoxyphenylimino)propanoate 
• 1039136-81-6 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl (E)-3,3,3-trifluoro-2-(4-methoxyphenylimino)propanoate 
• 1422252-88-7 2-(trimethylsilyl)ethyl 2-[(4-methoxyphenyl)amino]-2-(trifluoromethyl)-4-pentynoate 

Relevant academic research and scientific papers

Synthesis of fluorinated allylic amines: Reaction of 2-(trimethylsilyl)ethyl sulfones and sulfoxides with fluorinated imines

A new synthesis of fluorinated allylamines through the reaction of 2-(trimethylsilyl)ethyl sulfones and sulfoxides (as vinyl anion equivalents) with imines and imino esters has been described. The process includes a TBAF-mediated fragmentation of 2-(trime

Selective formal transesterification of fluorinated 2-(trimethylsilyl)ethyl α-imino esters mediated by TBAF

(Chemical Equation Presented) The scope of the transesterification reaction between β-fluorinated α-imino esters and various electrophiles in the presence of TBAF as fluorine source is described. The reaction is highly selective for alkyl iodides, bromide