Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov’t, Research Support, U.S. Gov’t, Non-P.H.S., Journal of the American Chemical Society called Intermolecular Hydroamination of 1,3-Dienes To Generate Homoallylic Amines, Author is Yang, Xiao-Hui; Lu, Alexander; Dong, Vy M., which mentions a compound: 2343-22-8, SMILESS is FC1=CC2=C(NCC2)C=C1, Molecular C8H8FN, Category: piperazines.
Authors report a Rh-catalyzed hydroamination of 1,3-dienes to generate homoallylic amines. The work show-cases the first case of anti-Markovnikov selectivity in the intermol. coupling of amines and 1,3-dienes. By tuning the ligand properties and Bronsted acid additive, it was found that a combination of rac-BINAP and mandelic acid is critical for achieving anti-Markovnikov selectivity.
From this literature《Intermolecular Hydroamination of 1,3-Dienes To Generate Homoallylic Amines》,we know some information about this compound(2343-22-8)Category: piperazines, but this is not all information, there are many literatures related to this compound(2343-22-8).
Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics