42984-30-5

Upstream product

• 126-81-8 dimedone 
• 75-04-7 ethylamine 

Downstream Products

• 76159-15-4 3-Ethylamino-2-hexamethyleniminomethyl-5,5-dimethyl-2-cyclohexen-1-on 
• 76159-30-3 2-(2-Ethylamino-4,4-dimethyl-6-oxo-1-cyclohexenylmethyl)-3-hydroxy-5,5-dimethyl-2-cyclohexen-1-on 
• 76159-29-0 2,2'-Methylen-bis(3-ethylamino-5,5-dimethyl-2-cyclohexen-1-on) 
• 76159-13-2 3-Ethylamino-5,5-dimethyl-2-piperidinomethyl-2-cyclohexen-1-on 
• 1467055-79-3 diethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate 
• 1467055-87-3 dimethyl 2-(2-(ethylamino)-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)-1H-benzo[d]imidazole-1,3(2H)-dicarboxylate 
• 1414998-38-1 6,6-dimethyl-2-picolinoyl-3-p-tolyl-6,7-dihydrobenzofuran-4(5H)-one 
• 1067646-92-7 1-ethyl-6,6-dimethyl-3-(5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-3-(trifluoromethyl)-3,5,6,7-tetrahydro-1H-indole-2,4-dione 
• 190207-44-4 1-ethyl-2-(4-methoxy-phenyl)-7,7-dimethyl-4-thioxo-4,6,7,8-tetrahydro-1H-quinazolin-5-one 
• 76159-18-7 2-Diethylaminomethyl-3-ethylamino-5,5-dimethyl-2-cyclohexen-1-on 
• 76159-17-6 2-Dimethylaminomethyl-3-ethylamino-5,5-dimethyl-2-cyclohexen-1-on 
• 80960-13-0 Toluene-4-sulfonate(2-ethylamino-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-phenyl-iodonium; 
• 76159-16-5 3-Ethylamino-5,5-dimethyl-2-morpholinomethyl-2-cyclohexen-1-on 
• 76159-14-3 3-Ethylamino-5,5-dimethyl-2-(1-pyrrolidinylmethyl)-2-cyclohexen-1-on 

Relevant academic research and scientific papers

Metal-free syntheses of new azocinesviaaddition reactions of enaminones with acenaphthoquinone followed by oxidative cleavages of the corresponding vicinal diols

A one-pot, clean and green procedure is described for the syntheses of new azocine derivativesviaaddition reactions of enaminones with acenaphthoquinone followed by periodic acid-mediated oxidative cleavages of the corresponding vicinal diols. Various derivatives of azocine were prepared and well characterized. The excellent yields, simple synthesis procedure, lack of a need to carry out any tedious work-up and column chromatography, metal-free catalysis, and mild reaction conditions are important features of this protocol.