In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Stereospecific Pd-Catalyzed Cross-Coupling Reactions of Secondary Alkylboron Nucleophiles and Aryl Chlorides, published in 2014-10-08, which mentions a compound: 1445086-17-8, mainly applied to secondary alkylboron arylchloride stereospecific cross coupling palladium catalyst, Related Products of 1445086-17-8.
We report the development of a Pd-catalyzed process for the stereospecific cross-coupling of unactivated secondary alkylboron nucleophiles and aryl chlorides. This process tolerates the use of secondary alkylboronic acids and secondary alkyltrifluoroborates and occurs without significant isomerization of the alkyl nucleophile. Optically active secondary alkyltrifluoroborate reagents undergo cross-coupling reactions with stereospecific inversion of configuration using this method.
Compounds in my other articles are similar to this one(P(t-Bu)3 Pd G3)Related Products of 1445086-17-8, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.
Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts