117794-75-9

Upstream product

• 58567-50-3 N-[2-(phenyl)prop-2-en-1-yl]-N-(p-toluenesulfonyl)amide 
• 106-95-6 allyl bromide 
• 127-65-1 chloroamine-T 
• 5155-87-3 3-phenylbut-3-enoic acid 
• 50487-71-3 4-methyl-N-(2-propenyl)benzenesulfonamide 
• 3360-54-1 3-bromo-2-phenylprop-1-ene 
• 56865-69-1 N-allyl-2-phenylprop-2-en-1-amine 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 50487-71-3 4-methyl-N-(2-propenyl)benzenesulfonamide 
• 7283-47-8 (4,4-dimethylpent-1-en-2-yl)benzene 
• 877614-77-2 3-phenyl-1-p-toluenesulfonyl-1,2,5-trihydropyrrole 

Relevant academic research and scientific papers

Iodine-Catalyzed Decarboxylative Amidation of β,γ-Unsaturated Carboxylic Acids with Chloramine Salts Leading to Allylic Amides

The iodine-catalyzed decarboxylative amidation of β,γ-unsaturated carboxylic acids with chloramine salts is described. This method enables the regioselective synthesis of allylic amides from various types of β,γ-unsaturated carboxylic acids containing sub

Highly flexible synthesis of chiral azacycles via iridium-catalyzed hydrogenation

A range of saturated chiral azacycles has been prepared in high yield and with high selectivity from simple starting materials. A modular approach with ring-closing metathesis as a key step was used to produce a number of five-, six-, and seven-membered c

2-Arylallyl as a new protecting group for amines, amides and alcohols

Amines, amides and ethers containing 2-arylallyl groups are selectively and easily deprotected with tert-butyllithium. This transformation probably involves a carbolithiation reaction of the styrenyl moiety followed by a β-elimination process. The Royal Society of Chemistry 2005.