676591-83-6

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 312329-87-6 N-ethynyl-N-phenyl-4-methyl-benzenesulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 62-53-3 aniline 
• 68-34-8 phenyl toluenesulfonamide 
• 1066-54-2 trimethylsilylacetylene 
• 312329-83-2 N-(2,2-dichlorovinyl)-N-phenyl-4-methyl-benzenesulfonamide 

Downstream Products

• 1337936-30-7 4-methyl-N-octa-1,3-diynyl-N-phenylbenzenesulfonamide 
• 1337936-58-9 N-(5-(hex-1-yn-1-yl)-2-phenyloxazol-4-yl)-4-methyl-N-phenylbenzenesulfonamide 
• 1429481-71-9 1-(toluene-4-sulfonyl)-1,3-dihydro-indol-2-one 
• 68-34-8 phenyl toluenesulfonamide 
• 84672-52-6 N-acetyl-N-phenyl-p-toluenesulfonamide 
• 1262669-96-4 2-oxo-N, 2-diphenyl-N-tosylacetamide 

Relevant academic research and scientific papers

Synthesis of disubstituted ynamides from β,β-dichloroenamides and electrophiles

Treatment of β,β-dichloroenamides with n-butyllithium, followed by addition of an electrophile, provides disubstituted ynamides in far greater yield than direct functionalization of terminal ynamides. Georg Thieme Verlag Stuttgart.

Synthesis of Oxindoles through the gold-catalyzed oxidation of N-arylynamides

α-Oxo gold carbenoids generated by the oxidation of N-arylynamides can be trapped intramolecularly at the ortho position of the aryl ring to give functionalized oxindoles under mild reaction conditions. Pyridine N-oxide works as the oxidant, ligand, and base in this transformation. Copyright

Intermolecular and selective synthesis of 2,4,5-trisubstituted oxazoles by a gold-catalyzed formal [3+2] cycloaddition

Oxazole new world: A gold-catalyzed intermolecular reaction of pyridine-N-aminides with ynamides can be used to prepare trisubstituted 1,3-oxazoles with a variety of functional groups. This formal [3+2] cycloaddition employs robust conjugated N-ylides as

Coupling and cycloaddition of ynamides: Homo- and Negishi coupling of tosylynamides and intramolecular [4 + 2] cycloaddition of N-(o-ethynyl)phenyl ynamides and arylynamides

N,N′-aryl- and N,N′-alkyl-buta-1,3-diyne-1,4-ditosylamides have been synthesized for the first time, in good to excellent yields, by copper-catalyzed dimerization of the corresponding N-aryl or N-alkyl tosylynamides. Negishi coupling of N-ethynylzinc tosy

Homocoupling of 1-Alkynyl Tosylamides

N,N′-substituted-buta-1,3-diyne-1,4-tosylamides have been synthesized for the first time, in good to excellent yields, via copper-catalyzed dimerization of the corresponding 1-alkynyltosylamides.