Reference of 301673-14-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.301673-14-3, Name is tert-Butyl 4-iodopiperidine-1-carboxylate, molecular formula is C10H18INO2. In a Article，once mentioned of 301673-14-3
Selective catalytic synthesis of Z-olefins has been challenging. Here we describe a method to produce 1,2-disubstituted olefins in high Z selectivity via reductive cross-coupling of alkyl halides with terminal arylalkynes. The method employs inexpensive and nontoxic catalyst (iron(II) bromide) and reductant (zinc). The substrate scope encompasses primary, secondary, and tertiary alkyl halides, and the reaction tolerates a large number of functional groups. The utility of the method is demonstrated in the synthesis of several pharmaceutically relevant molecules. Mechanistic study suggests that the reaction proceeds through an iron-catalyzed anti-selective carbozincation pathway.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Reference of 301673-14-3, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 301673-14-3
Reference：
Piperidine – Wikipedia,
Piperidine | C5H23432N – PubChem