142095-77-0Relevant articles and documents
Pd(0)-catalyzed chemoselective construction of spirocarbocycles via an alkyne insertion/β-naphthol dearomatization cascade
Zheng, Huayu,Bai, Lu,Liu, Jingjing,Nan, Jiang,Zuo, Zhijun,Yang, Liu,Wang, Yaoyu,Luan, Xinjun
, p. 3061 - 3064 (2015/06/08)
A microwave-assisted Pd(0)-catalyzed alkyne migratory insertion/β-naphthol dearomatization cascade process has been accomplished to access a variety of spirocyclic compounds bearing all-carbon quaternary stereogenic centers in high yields with excellent chemoselectivities.
The reactivity of oxygen nucleophiles with aryl radicals in the S(RN)1 mechanism
Baumgartner,Pierini,Rossi
, p. 2323 - 2326 (2007/10/02)
The photostimulated reaction of 2-naphthoxide ions 1 with o-dihalobenzenes in liquid ammonia gives the halosubstituted product 4 and the cyclized substituted product 5. This is the first report about the coupling of an aromatic σ radical with an oxygen functionality in the chain propagation cycle of the S(RN)1 mechanism.