19821-21-7Relevant articles and documents
Price et al.
, p. 2760 (1939)
Novel α-arylnitriles synthesis via Ni-catalyzed cross-coupling of α-bromonitriles with arylboronic acids under mild conditions
Yang, Yingying,Tang, Shan,Liu, Chao,Zhang, Huimin,Sun, Zhexun,Lei, Aiwen
supporting information; experimental part, p. 5343 - 5345 (2011/09/13)
An applicable and easy-handling Ni-catalyst can be used to promote direct arylation of α-bromonitriles with various arylboronic acids to construct α-arylnitriles under mild conditions. The methodology tolerates β-hydrogens and functional groups in the substrates.
Aryne insertion into α-cyanocarbonyl compounds: Direct introduction of carbonyl and cyanomethyl moieties into the aromatic skeletons
Yoshida, Hiroto,Watanabe, Masahiko,Ohshita, Joji,Kunai, Atsutaka
, p. 6729 - 6731 (2007/10/03)
Two different carbon functional groups can be introduced simultaneously into 1,2-positions of aromatic skeletons based upon a novel insertion reaction of arynes into a carbonyl-cyanomethyl σ-bond of α-cyanocarbonyl compounds.
