863403-17-2

Upstream product

• 863403-16-1 (+)-(R)-(E)-ethyl 5-(4-methoxyphenyl)-4-(toluene-4-sulfonamido)pent-2-enoate 
• 863403-09-2 (+)-(R)-2-(toluene-4-sulfonamido)-3-(4-methoxyphenyl)propan-1-ol 
• 863403-15-0 (+)-(S)-3-hydroxy-1-(4-methoxyphenyl)-2-(toluene-4-sulfonamido)propan-1-one 
• 7663-92-5 N-tosyl-L-serine 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 863403-10-5 (R)-(E)-5-(4-methoxyphenyl)-4-(4-methylbenzylamino)pent-2-en-1-ol 
• 863403-18-3 (+)-(R)-(E)-5-(4-methoxyphenyl)-4-{(4-methylbenzyl)[(toluene-4-sulfonyl)acetyl]amino}pent-2-enol 
• 863403-08-1 (+)-(R)-(E)-carbonic acid 5-(4-methoxyphenyl)-4-[(4-methylbenzyl)-2-(toluene-4-sulfonyl)acetylamino]pent-2-enyl ester methyl ester 
• 863403-38-7 (R)-(E)-4-amino-5-(4-methoxyphenyl)pent-2-en-1-ol 

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.