17102-73-7

Upstream product

• 64-18-6 formic acid 
• 1150-26-1 N-(4-Methoxy-phenyl)-4-methyl-benzenesulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 104-94-9 4-methoxy-aniline 
• 72773-04-7 N-formylbenzotriazole 
• 4885-02-3 Dichloromethyl methyl ether 

Downstream Products

• 853688-09-2 N-(2,2-dichlorovinyl)-N-(4-methoxyphenyl)-4-methylbenzenesulfonamide 
• 950777-61-4 N-(4-methoxyphenyl)-N-((E)-3-hydroxyprop-1-enyl)-4-methylbenzenesulfonamide 
• 853688-18-3 N-(2-chloro-2-phenyl-vinyl)-N-(4-methoxy-phenyl)-4-methyl-benzenesulfonamide 

Relevant academic research and scientific papers

Synthesis of 1,2-amino alcohols by sigmatropic rearrangements of 3-(N-Tosylamino)allylic alcohol derivatives

Sigmatropic rearrangements of 3-(N-tosylamino)allylic alcohol derivatives, a particular subclass of functionalized enamides, have been investigated. Whereas the presence of the nitrogen atom alters the stereochemical outcome of Ireland-Claisen rearrangeme

Palladium-catalyzed Suzuki-Miyaura coupling reactions involving β,β-dihaloenamides: Application to the synthesis of disubstituted ynamides

β,β-Dihaloenamides can be successfully involved in palladium-catalyzed Suzuki-Miyaura coupling reactions. Whereas the resulting tri substituted (Z)-β-bromoenamides could participate in a second cross-coupling leading to β,β-disubstituted enamides, the (Z)-β-chloroenamides have been converted to disubstituted ynamides by an E2 elimination.