More research is needed about 1-(4-Trifluoromethylphenyl)piperidine-4-carboxylic acid

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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, 607354-69-8, molcular formula is C13H14F3NO2, introducing its new discovery. Safety of 1-(4-Trifluoromethylphenyl)piperidine-4-carboxylic acid

Base-Controlled Diastereoselective Synthesis of Either anti- or syn-beta-Aminonitriles

Deprotonation of secondary alkane nitriles with nBuLi and addition to aryl imines gives kinetic anti-beta-aminonitriles. Use of LHMDS allows reversible protonation of the reaction intermediate to give syn-beta-aminonitriles. The pure diastereosiomers can be isolated in good yields, and the mechanism was elucidated.

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H22267N – PubChem