Transition-metal-free intramolecular N-arylations.
Isabelle Thomé, Carsten Bolm
Index: Org. Lett. 14(7) , 1892-5, (2012)
Full Text: HTML
Abstract
N-Substituted phenoxazines and related aza analogs have been prepared from N-acetylated aryloxy anilides by transition-metal-free, base-catalyzed cyclization reactions. In the presence of a mixture of 10 mol % of N,N'-dimethylethylenediamine (DMEDA) and 2 equiv of K(2)CO(3) in toluene at 135 °C the products are obtained in high yields.
Related Compounds
Related Articles:
2015-06-30
[Oncotarget 6 , 16488-506, (2015)]
2007-10-01
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 68(2) , 394-8, (2007)]
2012-06-01
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 91 , 383-8, (2012)]
2009-02-01
[Chem. Pharm. Bull. 57(2) , 211-3, (2009)]
2006-03-03
[J. Org. Chem. 71(5) , 1802-8, (2006)]