Electric Literature of 211108-50-8, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.211108-50-8, Name is tert-Butyl 3-fluoro-4-oxopiperidine-1-carboxylate, molecular formula is C10H16FNO3. In a article，once mentioned of 211108-50-8
A Rh(III)-catalyzed addition of benzylic C(sp3)-H bond to alpha,beta-unsaturated ketones/aldehydes has been realized, leading to efficient synthesis of gamma-aryl ketones/aldehydes. This atom-economic reaction proceeded under mild and redox-neutral conditions with a broad substrate scope. Besides benzylic C-H, allylic C-H bonds are also applicable when assisted by O-methyl ketoxime directing groups.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 211108-50-8, and how the biochemistry of the body works.Electric Literature of 211108-50-8
Reference：
Piperidine – Wikipedia,
Piperidine | C5H17582N – PubChem