1438047-98-3

Upstream product

• 32462-30-9 (S)-hydroxyphenylglycine 
• 111524-99-3 N-(p-tolylsulfonyl)-α-phenylglycine chloride 
• 618-36-0 rac-methylbenzylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 111524-98-2 (2S)-2-phenyl-2-(tosylamino)acetic acid 

Relevant academic research and scientific papers

Synthetically amenable amide derivatives of tosylated-amino acids as organocatalysts for enantioselective allylation of aldehydes: Computational rationale for enantioselectivity

A phenylalanine derived chiral amide is developed that serves as an effective organocatalyst for the reaction of allyltrichlorosilane with aryl, hetero-aryl and α,β-unsaturated aldehydes to afford the desired homoallylic alcohols in good yield (up to 90%)