1350810-15-9

Upstream product

• 1504-58-1 3-Phenyl-2-propyn-1-ol 
• 70-55-3 toluene-4-sulfonamide 
• 222421-22-9 (Z)-3-iodo-2-phenyl-3-phenylprop-2-en-1-ol 
• 100-58-3 phenylmagnesium bromide 

Downstream Products

• 1350809-99-2 C₂₅H₂₄N₂O₃S 
• 1350810-09-1 4,5-diphenyl-1-tosyl-1,6-dihydropyridin-3(2H)-one 
• 1350810-26-2 C₂₄H₂₂INO₃S 
• 1350809-89-0 C₂₅H₂₅IN₂O₃S 
• 1350810-20-6 C₂₈H₃₂INO₄S 
• 1585185-91-6 C₂₅H₂₂INO₂S 
• 1585185-70-1 C₂₆H₂₅NO₃S 
• 1585185-84-7 C₂₅H₂₂INO₂S 
• 1394159-25-1 C₂₉H₃₁NO₄S 

Relevant academic research and scientific papers

Palladium-catalyzed cyclization of vinyl iodide-tethered allensulfonamide

This Letter describes a palladium-catalyzed cyclization of vinyl iodide-tethered allensulfonamide in the presence of alkylol, which provides a facile access to 2-alkoxy-3-methylene-tetrahydropyridine. The asymmetric version of this reaction has also been preliminarily realized with up to 81% enantioselectivity when chiral bisphosphine ligands were used.

Synthesis of 3-pyrroline via domino Heck-aza-Michael reaction

This Letter describes the Pd(0)-catalyzed domino Heck-aza-Michael reaction between (Z)-N-(3-iodoallyl)-tosylamide and acrylic ester. The reaction provides a facile access to an important class of substituted 3-pyrroline.

Palladium-catalyzed Heck-type reaction of oxime ether bearing a pendant vinyl iodide moiety

A Pd(0)-catalyzed intramolecular Heck-type reaction of oxime ether has been developed, providing convenient access to heterocyclic oximes. The Royal Society of Chemistry 2011.