@article{bailey_gagné_booker-milburn_houlden_ford_lloyd-jones_2008, 
  title={Distinct Reactivity of Pd(OTs) 2 : The Intermolecular Pd(II)-Catalyzed 1,2-Carboamination of Dienes}, 
  DOI={10.17615/yvd8-s387}, 
  abstractNote={A Pd-catalyzed intermolecular 1,2-carboamination route to indolines from N-aryl ureas and 1,3-dienes that proceeds under mild conditions in relatively nonacidic media, is presented. The in situ generation, or preformation, of a palladium tosylate emerges as a key parameter in gaining the requisite reactivity for the C-H insertion/carbopalladation/nucleophilic displacement process.}, 
  publisher={The University of North Carolina at Chapel Hill University Libraries}, 
  author={Bailey and Gagné and Booker-Milburn and Houlden and Ford and Lloyd-Jones}, 
  year={2008}
  }