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, Chemistry – A European Journal called Alkyne Aminopalladation/Heck and Suzuki Cascades: An Approach to Tetrasubstituted Enamines, Author is Geffers, Finn J.; Kurth, Florens R.; Jones, Peter G.; Werz, Daniel B., which mentions a compound: 175136-62-6, SMILESS is FC(C1=CC(C(F)(F)F)=CC(P(C2=CC(C(F)(F)F)=CC(C(F)(F)F)=C2)C3=CC(C(F)(F)F)=CC(C(F)(F)F)=C3)=C1)(F)F, Molecular C24H9F18P, Electric Literature of C24H9F18P.
Alkyne aminopalladation reactions starting from tosylamides, e.g., (E)-N-(5-(2-(but-2-en-1-yloxy)phenyl)pent-4-yn-1-yl)-4-Me N-((perfluorobenzoyl)oxy)benzenesulfonamide are reported. The emerging vinylic Pd species are converted either in an intramol. Heck reaction with olefinic units or in an intermol. Suzuki reaction by using boronic acids RB(OH)2 (R = C6H5, 4-ClC6H4, 2-thienyl, etc.) exhibiting broad functional group tolerance. Tetra(hetero)substituted tosylated enamines, e.g., I are obtained in a simple one-pot process.
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Reference:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem