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, Non-U.S. Gov’t, Research Support, N.I.H., Extramural, Journal of the American Chemical Society called Regioselective Arylboration of Isoprene and Its Derivatives by Pd/Cu Cooperative Catalysis, Author is Smith, Kevin B.; Brown, M. Kevin, which mentions a compound: 1445086-17-8, SMILESS is CC(C)(C)P(C(C)(C)C)([Pd+2]1([C-]2=CC=CC=C2C3=CC=CC=C3N1)[O-]S(C)(=O)=O)C(C)(C)C, Molecular C25H40NO3PPdS, Safety of P(t-Bu)3 Pd G3.
A method for the regioselective arylboration of isoprene and its derivatives is presented. These reactions allow for the synthesis of useful building blocks from simple components. Through these studies, an unusual additive effect with DMAP was uncovered that allows for altered reactivity and the formation of quaternary C centers. The utility of this method is demonstrated toward the formal synthesis of mesembrine.
As far as I know, this compound(1445086-17-8)Safety of P(t-Bu)3 Pd G3 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.
Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts