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Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.name: (S)-2-Phenylpiperidine, you can also check out more blogs about70665-05-3

Chemistry is traditionally divided into organic and inorganic chemistry. name: (S)-2-Phenylpiperidine. The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent，Which mentioned a new discovery about 70665-05-3

(S)- and (R)-2-Phenylpiperidines, (S)- and (R)-2-methylpiperidines, meso- and (2R, 6R)-2,6-diphenylpiperidines, and meso- and (25, 65)-2,6-dimethylpiperidines were synthesized asymmetrically starting from the diastereoselective addition of Grignard reagents to chiral 1,3-oxazolidines, converting of 1-aza-4-oxabicyclo[4.3.0]nonane derivatives as pivotal intermediates.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.name: (S)-2-Phenylpiperidine, you can also check out more blogs about70665-05-3

Reference：
Piperidine – Wikipedia,
Piperidine | C5H9369N – PubChem