24953-56-8Relevant academic research and scientific papers
Cu(II)-Catalyzed Construction of Heterobiaryls using 1-Diazonaphthoquinones: A General Strategy for the Synthesis of QUINOX and Related P,N Ligands
Biswas, Aniruddha,Pan, Subarna,Samanta, Rajarshi
, p. 1631 - 1636 (2022/03/14)
An efficient and straightforward method was developed for the synthesis of heterobiaryls using easily available N-oxides and diazonaphthoquinones under cheap Cu(II) catalysis. The developed method offered QUINOX and related congeners in a simple manner. A wide scope of important heterobiaryls was achieved with high site selectivity. The synthesized naphthols were transformed into the privileged related P,N ligands. Suitable resolution methods can directly afford the corresponding axially chiral heterobiaryls.
Preparation of heteroaryloxetanes and heteroarylazetidines by use of a Minisci reaction
Duncton, Matthew A. J.,Estiarte, M. Angels,Johnson, Russell J.,Cox, Matthew,O'Mahony, Donogh J. R.,Edwards, William T.,Kelly, Michael G.
supporting information; experimental part, p. 6354 - 6357 (2009/12/08)
(Chemical Equation Presented) Introduction of oxetan-3-yl and azetidin-3-yl groups into heteroaromatic bases was achieved by using a radical addition method (Minisci reaction). To demonstrate utility, the process was used to introduce an oxetane or azetid
