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, 34737-89-8, Name is 1-Benzyl-3-methylpiperidin-4-one, SMILES is O=C1C(C)CN(CC2=CC=CC=C2)CC1, in an article , author is Devi, Ngangbam Renubala, once mentioned of 34737-89-8, Formula: C13H17NO.
Synthesis of 4-Vinyl-1,2,3,4-tetrahydroisoquinoline from N-Tethered Benzyl-Alkenol Catalyzed by Indium(III) Chloride: Formal Synthesis of (+/-)-Isocyclocelabenzine
An intramolecular Friedel-Crafts cyclization reaction catalyzed by indium(III) chloride for the formation of 4-vinyl-1,2,3,4-tetrahydroisoquinoline from N-tethered benzyl-alkenol in good yields has been described. The reaction is highly regioselective and generates an exocyclic vinyl functionality in the piperidine ring. The reaction is compatible with a wide range of functional groups. The strategy is demonstrated for the formal synthesis of (+/-)-isocyclocelabenzine alkaloid.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 34737-89-8, you can contact me at any time and look forward to more communication. Formula: C13H17NO.
Reference:
Piperidine – Wikipedia,
,Piperidine | C5H11N – PubChem