64771-37-5

Upstream product

• 106013-78-9 2-Dimethylamino-4-methyl-5-phenyl-[1,3]oxazin-6-one 
• 108471-67-6 ((Z)-2-Dimethylcarbamoyl-1-methyl-2-phenyl-vinyl)-carbamic acid methyl ester 
• 18925-69-4 N,N-dimethyl-2-phenylacetamide 
• 141-78-6 ethyl acetate 
• 33127-03-6 N,N-Dimethyl-2-phenylbutyramid 

Relevant academic research and scientific papers

Chemoselective formal β-functionalization of substituted aliphatic amides enabled by a facile stereoselective oxidation event

Aliphatic C-H functionalization is a topic of current intense interest in organic synthesis. Herein, we report that a facile and stereoselective dehydrogenation event enables the functionalization of aliphatic amides at different positions in a one-pot fa

Pd(II)-catalyzed synthesis of indoles from α-aryloxime O-pentafluorobenzoates via intramolecular aromatic C-H amination

α-Aryl-a-aminocarbonyloxime O-pentafluorobenzoates are found to be promising precursors for synthesis of 2 3-disubstituted indole derivatives catalyzed by PdCl2(MeCN)2 in the presence of MgO as a base. The reaction is supposed to pro

The Vilsmeier-Haack Reaction of Isoxazolin-5-ones. Synthesis and Reactivity of 2-(Dialkylamino)-1,3-oxazin-6-ones

The Vilsmeier-Haack reaction on isoxazolin-5-ones gives 2-(dialkylamino)-1,3-oxazin-6-ones, and a reaction path is proposed depending on substitution pattern of the isoxazolin-5-ones studied.A thermal equilibrium between the oxazinones, imino ketenes, and vinyl isocyanates is hypothesized to explain most of the chemical reactivity of the 2-(dialkylamino)-1,3-oxazin-6-ones.