204857-48-7

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 204857-35-2 N-(tert-butoxycarbonyl)-N-(4-chlorobenzyl)-methanesulfonamide 
• 104-55-2 3-phenyl-propenal 
• 42060-30-0 N-(4-chloro-benzyl)-methanesulfonamide 
• 104-86-9 4-chlorobenzylamine 

Downstream Products

• 329010-42-6 (1E,3E)-4-Phenyl-buta-1,3-diene-1-sulfonic acid but-3-enyl-(4-chloro-benzyl)-amide 
• 329010-38-0 (1E,3E)-4-Phenyl-buta-1,3-diene-1-sulfonic acid allyl-(4-chloro-benzyl)-amide 

Relevant academic research and scientific papers

Synthesis of Cyclic Sulfonamides through Intramolecular Diels-Alder Reactions

(Matrix Presented) Substituted 2,3,3a,4,5,7a-hexahydrobenzo[d]isothiazole 1,1-dioxides and 3,4,4a,5,6,8a-hexahydro-2H-benzo[e][1,2]thiazine 1,1-dioxides, novel cyclic sulfonamides, were synthesized by the thermal Diels-Alder reaction of triene derivatives

A convenient synthesis of N-alkyl-(E)-1-alkenesulfonamides

A series of vinylsulfonamides 3 has been synthesised through a condensation of N-Boc-methanesulfonamides 1 and aldehydes 2. O-Boc-2-hydroxyalkanesulfonamides were identified as intermediates, arising from N-O transfer of the Boc group. Elimination of OBoc gave the vinylsulfonamides.