Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 4062-60-6, molcular formula is C10H24N2, introducing its new discovery. Quality Control of: N1,N2-Di-tert-butylethane-1,2-diamine
alpha-Ketodicarboxylic Acid Chloride Imide Chlorides in the Synthesis of Heterocycles, III.- A Novel Wittig-Smiles Reaction.
N-Cyclohexyl-2,2-dimethyl-3-oxosuccinyl chloride imide chloride (1) reacts with methylenetriphenylphosphoranes affording 3-benzylidene-1-cyclohexyl-4,4-dimethyl-2,5-pyrrolidinediones 10 through a novel Wittig-Smiles mechanism.The structure of compound 10a is confirmed by X-ray diffraction analysis.When the ylide carbon carries a methyl or phenyl substituent, the Wittig-Smiles reaction fails, and cyclization results merely in the formation of 1-cyclohexyl-4,4-dimethyl-2,3,5-pyrrolidinetrione (4).
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Quality Control of: N1,N2-Di-tert-butylethane-1,2-diamine, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 4062-60-6
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Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI