134259-04-4Relevant articles and documents
Sequential 1,3-dipolar cycloaddition-palladium catalysed cyclisation. A powerful new tactical combination
Grigg, Ronald,Coulter, Thomas
, p. 1359 - 1362 (2007/10/02)
A new flexible tactical combination of a 1,3-dipolar cycloaddition of an in situ generated azomethine ylide followed by a palladium catalysed cyclisation is described. The two reactions can be carried out as a 1 pot procedure if desired. Four new stereoce