Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 29968-78-3, Name is 4-Nitrophenylethylamine hydrochloride, SMILES is NCCC1=CC=C([N+]([O-])=O)C=C1.[H]Cl, in an article , author is Okano, T, once mentioned of 29968-78-3, Quality Control of 4-Nitrophenylethylamine hydrochloride.
Addition-elimination reaction of highly electrophilic difluoroolefin, 5-difluoromethylene-3-pyrrolin-2-ones
1-Alkyl-5-difluoromethylene-3-pyrroline-2-ones 2 were generated from 1-alklyl-5-trifluoromethyl-3-pyrrolin-2-ones 1 via dehydrofluorination with methyllithium at -78 degrees C. Spontaneous addition-elimination reaction of 2 with enolate anion of 1 gave fluorinated pyrrolinonylmethylidenepyrrolinones 3.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 29968-78-3, you can contact me at any time and look forward to more communication. Quality Control of 4-Nitrophenylethylamine hydrochloride.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem