103656-73-1Relevant articles and documents
Bipyridine-Type Bidentate Auxiliary-Enabled Copper-Mediated ?C-H/C-H Biaryl Coupling of Phenols and 1,3-Azoles
Hirano, Koji,Kajiwara, Rikuo,Miura, Masahiro,Xu, Shibo
, p. 5405 - 5409 (2021)
A copper-mediated dehydrogenative C-H/C-H biaryl coupling of phenols and 1,3-azoles has been developed. The key to its success is the introduction of a bipyridine-type bidentate auxiliary, 4,4′-di(tert-butyl)-2,2′-bipyridine, on the phenol oxygen, which is readily prepared and easily attachable, detachable, and recyclable. The reaction proceeds smoothly in the presence of copper salt alone to form the corresponding phenol-azole heterobiaryls, which are prevalent motifs in functional molecules such as excited-state intramolecular proton transfer materials.
Simple and efficient preparation of 2,5-disubstituted oxazoles via a metal-free-catalyzed cascade cyclization
Wan, Changfeng,Gao, Linfeng,Wang, Qiang,Zhang, Jintang,Wang, Zhiyong
supporting information; experimental part, p. 3902 - 3905 (2010/11/04)
A practical and simple synthesis of 2,5-disubstituted oxazoles was developed via an iodine-catalyzed tandem oxidative cyclization. A wide range of common commercial aromatic aldehydes can be used as reaction substrates, which displayed excellent functional group compatibility in this reaction.