1039136-70-3

Upstream product

• 201230-82-2 carbon monoxide 
• 100-51-6 benzyl alcohol 
• 1039136-57-6 2-(trimethylsilyl)ethyl 3,3-difluoro-2-[(4-methoxyphenyl)imino]-5-hexenoate 
• 55791-06-5 benzyl mesylate 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 364049-82-1 N-(4-methoxyphenyl)-1-chloro-2,2-difluoro-4-pentenimidoyl chloride 
• 104-94-9 4-methoxy-aniline 
• 55039-89-9 2,2-difluoropent-4-enoic acid 

Downstream Products

• 911395-39-6 benzyl 3,3-difluoro-2-(4-methoxyphenyl)amino-2-(2-methylallyl)-5-hexenoate 
• 911395-36-3 benzyl 2-allyl-3,3-difluoro-2-(4-methoxyphenyl)amino-5-hexenoate 
• 1071527-52-0 (+/-)-benzyl 2-(1,1-difluorobut-3-enyl)-1-(4-methoxyphenyl)-4-methylene-5-oxopyrrolidine-2-carboxylate 
• 911395-48-7 benzyl 6,6-difluoro-1-[(4-methoxyphenyl)amino]-3-cyclohexene-1-carboxylate 

Relevant academic research and scientific papers

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

Asymmetric synthesis of new β,β-difluorinated cyclic quaternary α-amino acid derivatives

The synthesis of new β,β-difluorinated cyclic quaternary α-amino acid derivatives 1 in which a ring-closing metathesis reaction (RCM) constitutes the key step is described. The approach employs imidoyl chlorides 3 as fluorinated building blocks, and the o