Guan, Zhenhong published the artcileA highly efficient catalyst for Suzuki-Miyaura coupling reaction of benzyl chloride under mild conditions, Category: nitriles-buliding-blocks, the publication is RSC Advances (2014), 4(69), 36437-36443, database is CAplus.
Diarylmethane derivatives, were synthesized in Suzuki-Miyaura coupling reaction of benzyl chloride with arylboronic acids. Pd(II) organometallic catalysts immobilized on the triphenylphosphine-functionalized microporous knitting aryl polymer (KAPs(Ph-PPh3)-Pd) as a novel heterogeneous catalyst was employed in Suzuki-Miyaura coupling reaction of benzyl chloride and exhibited excellent catalytic activity under mild conditions with a turnover frequency (TOF) up to 76 min-1 (4569 h-1). This work reveals that the microporous structure of the catalyst can rapidly adsorb substrates, consequently facilitating their interaction, and eventually promoting the catalytic efficiency.
RSC Advances published new progress about 612-13-5. 612-13-5 belongs to nitriles-buliding-blocks, auxiliary class Organic Pigment, name is 2-(Chloromethyl)benzonitrile, and the molecular formula is C8H6ClN, Category: nitriles-buliding-blocks.
Referemce:
https://en.wikipedia.org/wiki/Nitrile,
Nitriles – Chemistry LibreTexts