758686-13-4

Upstream product

• 6590-65-4 N-(2-Formyl-phenyl)-4-methyl-benzenesulfonamide 
• 109-72-8 n-butyllithium 
• 31659-28-6 N-(2-Cyanophenyl)-4-methylbenzenesulfonamide 
• 941-55-9 4-toluenesulfonyl azide 
• 1009-14-9 phenyl butyl ketone 

Downstream Products

• 664981-87-7 N-[2-(1-n-hexyn-1-yl)phenyl]-4-methylbenzenesulfonamide 
• 1359966-82-7 C₂₆H₃₃NO₄S 

Relevant academic research and scientific papers

Ru(ii)-catalyzed intermolecular C-H amidation of weakly coordinating ketones

An efficient Ru(ii)-catalyzed intermolecular amidation of weakly coordinating ketones with sulfonyl azides via C-H bond activation is described. The reaction proceeds with high functional group tolerance, providing a novel approach to practical ketone-directed intermolecular C-N bond formation in the absence of an additional oxidant.

Hg(OTf)2-catalyzed vinylogous semi-pinacol rearrangement leading to 1,4-dihydroquinolines

An efficient method for the construction of dihydroquinoline derivatives possessing a quaternary carbon center is developed by an application of Hg(OTf)2-catalyzed vinylogous semi-pinacol-type rearrangement. The reaction was found to be specifi

One-pot synthesis of 2,3-disubstituted N-tosylindoles from o-acyl-N-tosylanilines

The reaction of oacyl-N-tosylanilines with lithium trimethylsilyldiazomethane followed by treatment with t-BuLi and then electrophiles gave 2,3-disubstituted N-tosylindoles in a one-pot process. Georg Thieme Verlag Stuttgart.