82994-21-6Relevant articles and documents
Synthesis of diaryl ethers with acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase inhibitory actions
?zbey, Fadime,Taslimi, Parham,Gül?in, ?lhami,Mara?, Ahmet,G?ksu, Süleyman,Supuran, Claudiu T.
, p. 79 - 85 (2016)
A series of diaryl ethers were synthesized and their human (h) carbonic anhydrase (CA) isoenzymes hCA I and II, acetylcholinesterase (AChE), and butyrylcholinesterase (BuChE) inhibitory actions were investigated. The new compounds were synthesized from th
Diaryl Ether Formation Merging Photoredox and Nickel Catalysis
Liu, Le,Nevado, Cristina
supporting information, p. 2188 - 2193 (2021/05/04)
Photoredox and Ni catalysis are combined to produce diaryl ethers under mild conditions. A broad range of aryl halides and phenol derivatives are cross-coupled in the presence of a readily available organic photocatalyst and NiBr2(dtbpy). Symmetrical diaryl ethers have also been directly obtained from aryl bromides in the presence of water. Mechanistic investigations support the involvement of Ni(0) species at the outset of the reaction and a Ni(II)/Ni(III)-photocatalyzed single electron transfer process preceding the productive C(sp2)-OAr reductive elimination.
Odd-numbered oxacalix[ n ]arenes (n = 5, 7): Synthesis and solid-state structures
Van Rossom, Wim,Robeyns, Koen,Ovaere, Magriet,Van Meervelt, Luc,Dehaen, Wim,Maes, Wouter
body text, p. 126 - 129 (2011/03/19)
The critical synthetic access to odd-numbered calix[n]arenes has evidently resulted in less attention for these macrocycles, although specific molecular recognition phenomena have been observed for some of them. A straightforward fragment coupling approac
