1052176-52-9Relevant academic research and scientific papers
Synthesis of aryl-substituted 1,4-dihydroquinolines by [4+2] cycloaddition of benzyne with 1-azadienes
Stokes, Sean,Bekkam, Markondaiah,Rupp, Madeline,Mead, Keith T.
supporting information; experimental part, p. 389 - 392 (2012/03/12)
The synthesis of aryl-substituted 1,4-dihydroquinolines can be achieved using a [4+2] cycloaddition between benzyne and various aryl-substituted 1-azadienes. The conditions are tolerated by N-aryl-, alkyl-, tosyl-, and tert-butoxycarbonyl-protected 1-azad
Oxidation of aliphatic α,β-unsaturated aldimines to amides specifically by oxone with AlCl3
Lu, Zhou,Peng, Lijun,Wu, Wentao,Wu, Longmin
, p. 2357 - 2366 (2008/09/21)
α,β-Unsaturated aldimines were specifically oxidized to amides with Oxone in the presence of AlCl3 as a Lewis acid in CH2Cl2. No migration of aryl group occurred in the rearrangement reaction. Copyright Taylor & Francis Group, LLC.
