132555-22-7Relevant articles and documents
Regioselective synthesis of 3-(2-hydroxyaryl)pyridines via arynes and pyridine N-oxides
Raminelli, Cristiano,Liu, Zhijian,Larock, Richard C.
, p. 4689 - 4691 (2006)
A variety of substituted 3-(2-hydroxyphenyl)pyridines have been prepared regioselectively by a transition-metal-free, mild, one-step route, which involves the reaction of pyridine N-oxides with silylaryl triflates in the presence of CsF in acetonitrile at
SRN1C-arylation of potassium aryloxides by arylazo phenyl or tert- butyl sulfides in DMSO
Petrillo, Giovanni,Novi, Marino,Dell Erba, Carlo,Tavani, Cinzia,Berta, Giovanni
, p. 7977 - 7990 (2007/10/02)
Aryloxide ions (Ar′O-) behave as C-nucleophiles towards diazosulfides (ArN = NSR; R = Ph, But) leading to imsymmetrical hydroxybiaryls (ArAr′OH) via C-C coupling. The reaction is particularly suited for the synthesis of terms which contain electron-withdrawing groups on the Ar moiety. The SRN1 mechanism is proposed on the grounds of experimental evidences.