TY  - JOUR
  - Kissane, M,McNamara, OA,Mitchell, D,Coppert, DM,Moynihan, HA,Lorenz, KT,Maguire, AR
  - 2012
  - January
  - Tetrahedron Letters
  - Expanded scope of heterocyclic biaryl synthesis via a palladium-catalysed thermal decarboxylative cross-coupling reaction
  - Validated
  - ()
  - Cross-coupling Palladium Heterocycles Biaryls Aryl halides HETEROAROMATIC CARBOXYLIC-ACIDS ARYL HALIDES ARENECARBOXYLIC ACIDS AROMATIC CARBOXYLATES SALTS
  - 53
  - 403
  - 405
  - The palladium-catalysed decarboxylative cross-coupling of heterocyclic aromatic carboxylates and aryl halides is described. The cross-coupling proceeds under relatively mild conditions using catalytic Pd(0) and tetrabutylammonium bromide (TBAB). Utilizing a mixed solvent system consisting of N,N-dimethylformamide (DMF) and N-methyl-2-pyrrolidone (NMP), the cross-coupling system operated at temperatures ranging from 80 to 140 degrees C. (C) 2011 Elsevier Ltd. All rights reserved.
  - DOI 10.1016/j.tetlet.2011.11.051
DA  - 2012/01
ER  - 

@article{V160747961,
   = {Kissane,  M and McNamara,  OA and Mitchell,  D and Coppert,  DM and Moynihan,  HA and Lorenz,  KT and Maguire,  AR },
   = {2012},
   = {January},
   = {Tetrahedron Letters},
   = {Expanded scope of heterocyclic biaryl synthesis via a palladium-catalysed thermal decarboxylative cross-coupling reaction},
   = {Validated},
   = {()},
   = {Cross-coupling Palladium Heterocycles Biaryls Aryl halides HETEROAROMATIC CARBOXYLIC-ACIDS ARYL HALIDES ARENECARBOXYLIC ACIDS AROMATIC CARBOXYLATES SALTS},
   = {53},
  pages = {403--405},
   = {{The palladium-catalysed decarboxylative cross-coupling of heterocyclic aromatic carboxylates and aryl halides is described. The cross-coupling proceeds under relatively mild conditions using catalytic Pd(0) and tetrabutylammonium bromide (TBAB). Utilizing a mixed solvent system consisting of N,N-dimethylformamide (DMF) and N-methyl-2-pyrrolidone (NMP), the cross-coupling system operated at temperatures ranging from 80 to 140 degrees C. (C) 2011 Elsevier Ltd. All rights reserved.}},
   = {DOI 10.1016/j.tetlet.2011.11.051},
  source = {IRIS}
}