114877-80-4

Upstream product

• 32704-22-6 2-allyl-phenylamine 
• 114877-77-9 (3R,5R)-3-(tert-Butyl-diphenyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-dihydro-furan-2-one 
• 114877-77-9 (3S,5S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-dihydro-furan-2-one 

Downstream Products

• 114904-27-7 (2R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2,5-bis-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid (2-allyl-phenyl)-amide 
• 114877-87-1 (2S,4S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,5-bis-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid 
• 114904-27-7 (2S,4S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,5-bis-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid (2-allyl-phenyl)-amide 
• 114877-87-1 (2S,4S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,5-bis-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid 

Relevant academic research and scientific papers

Application of (Chloromethyl)aluminum 2-(2-Propenyl)anilide in the Conversion of γ- and δ-Lactones into Protected Hydroxy Acids

A series of γ- and δ-lactones including several aldonolactones were reacted with (chloromethyl)aluminum 2-(2-propenyl)anilide to produce the corresponding hydroxy amides.Protection using methyl chloride, (2-methoxyethoxy)methyl chl

CHLOROMETHYLALUMINUM 2-(2-PROPENYL)ANILIDE - A CONVENIENT REAGENT FOR THE CONVERSION OF LACTONES INTO PROTECTED HYDROXY ACIDS

The title reagent reacts with γ and δ lactones to provide hydroxy amides which can be easily converted into protected N-acyl indoles.Mild saponification provides indole and the protected hydroxy acid.