114877-83-7

Upstream product

• 3970-21-6 2-Methoxyethoxymethyl chloride 
• 114904-26-6 (2R,3R,4R)-2,3,5-Tris-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-pentanoic acid (2-allyl-phenyl)-amide 
• 114904-26-6 (2R,3R,4R)-2,3,5-Tris-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-pentanoic acid (2-allyl-phenyl)-amide 
• 92512-25-9 (3R,4R,5R)-3,4-bis((tert-butyldimethylsilyl)oxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)dihydrofuran-2(3H)-one 
• 32704-22-6 2-allyl-phenylamine 
• 92512-25-9 (3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-dihydro-furan-2-one 

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.