335004-44-9

Upstream product

• 821-06-7 (E)-1,4-dibromobutene 
• 18303-04-3 N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide 
• 24424-99-5 di-tert-butyl dicarbonate 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 335004-51-8 (E,E)-1,11-bis(tert-butyloxycarbonyl)-1,6,11-tris[(4-methylphenyl)sulfonyl]-1,6,11-triazaundeca-3,8-diene 
• 540744-15-8 di(tert-butyl) N-{(2E)-4-{[(tert-butoxy)carbonyl][(4-methylphenyl)sulfonyl]amino}but-2-enyl}imidodicarbonate 
• 540744-13-6 tert-butyl [(2E)-4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)but-2-enyl][(4-methylphenyl)sulfonyl]carbamate 
• 935748-88-2 (-)-(S)-(N-2-methylbut-3-enyl)(N-t-butoxycarbonyl)p-toluenesulfonamide 
• 945082-49-5 (E,E,E)-1,16-bis(tert-butyloxycarbonyl)-1,6,11,16-tetrakis[(4-methylphenyl)sulfonyl]-1,6,11,16-tetraazahexadeca-3,8,13-triene 
• 945082-78-0 (E,E,E,E,E)-1,26-bis(tert-butyloxycarbonyl)-1,6,11,16,21,26-hexakis[(4-methylphenyl)sulfonyl]-1,6,11,16,21,26-hexaazahexacosa-3,8,13,18,23-pentaene 
• 335004-55-2 (E,E)-1,6,11-tris[(4-methylphenyl)sulfonyl]-1,6,11-triazaundeca-3,8-diene 
• 540744-14-7 N-[(2E)-4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-but-2-enyl]-4-methylbenzenesulfonamide 
• 949162-93-0 (E)-dimethyl 9-(p-toluenesulfonyl)-9-azatridec-6-ene-1,11-diyne-4,4-dicarboxylate 
• 949197-75-5 C₁₉H₂₃NO₆S 

Relevant academic research and scientific papers

The macrocyclic spermidine alkaloid (-)-(S)-neoperiphylline: Revision of the structure based on the total synthesis

The total synthesis of the two isomeric macrocyclic enamides 2 and 17 is described. The precursor 14 was synthesized by means of template-assisted macrocyclization (Scheme 2). Isomerization of 14 in the presence of [Fe(CO)5] gave 2 and 17 (Sche

Synthesis, catalytic activity and redox properties of palladium(0) complexes with 15-membered triolefinic macrocyclic ligands containing one, two or three ferrocenyl groups

A series of 15-membered triolefinic macrocycles containing ferrocenyl groups and their palladium(0) complexes have been synthesized and characterized. Their catalytic activity has been demonstrated in Suzuki-type cross-coupling and in the Heck reaction. Their redox properties have been investigated by means of cyclic voltammetry.

Preparation of nitrogen-containing 15-membered triolefinic macrocycles: (E,E,E)-1,6,11-tris(arylsulfonyl)-1,6,11-triazacyclopentadeca-3,8,13-trienes

Three routes to (E,E,E)-1,6,11-tris(arylsulfonyl)-1,6,11-triazacyclopentadeca-3,8,13-trienes are described. Optimization of the preparation of key intermediates has opened the way to efficient synthesis of a broad variety of 15-membered, nitrogen-containing triolefinic macrocycles.