863403-25-2

Upstream product

• 17360-25-7 N-(p-toluenesulfonyl)-L-valine 
• 139192-48-6 (S)-N-(1-hydroxy-3-methylbutan-2-yl)-4-methylbenzenesulfonamide 
• 753420-62-1 (E)-(S)-4-Amino-5-methyl-hex-2-en-1-ol 
• 104-87-0 4-methyl-benzaldehyde 
• 72-18-4 L-valine 
• 863403-20-7 (-)-(S)-(E)-ethyl 5-methyl-4-(toluene-4-sulfonamido)hex-2-enoate 
• 863403-23-0 (-)-(S)-(E)-5-methyl-4-(toluene-4-sulfonamido)hex-2-en-1-ol 
• 887113-19-1 4-methyl-N-[(2S)-3-methyl-1-oxobutan-2-yl]benzenesulfonamide 

Downstream Products

• 863403-29-6 (-)-(S)-(E)-5-methyl-4-{(4-methylbenzyl)[2-(toluene-4-sulfonyl)acetyl]amino}hex-2-enol 
• 863403-31-0 (-)-(S)-(E)-carbonic acid methyl ester 5-methyl-4-{(4-methylbenzyl)-[2-(toluene-4-sulfonyl)acetyl]amino}hex-2-enyl ester 

Relevant academic research and scientific papers

Stereoselective γ-lactam synthesis via palladium-catalysed intramolecular allylation

A novel route to the synthesis of 3-(tolylsulfonyl)-4,5-cis-disubstituted γ-lactams using a diastereoselective palladium-catalysed intramolecular allylation of amino acid-derived allylic carbonates has been developed. The Royal Society of Chemistry 2005.