4.8 Article

Improved functional group compatibility in the palladium-catalyzed synthesis of aryl amines

Journal

ORGANIC LETTERS
Volume 4, Issue 17, Pages 2885-2888

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol0262688

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Funding

  1. NCI NIH HHS [T32CA09112] Funding Source: Medline
  2. NIGMS NIH HHS [GM58160] Funding Source: Medline

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[GRAPHIC] The use of Pd(2)dba(3) with bulky, electron-rich ligands 1 or 2 and LIN(TMS)(2) as the base for the coupling of amines with aryl halides containing hydroxyl, amide, or enolizable keto groups is described. This protocol expands the utility of palladium-catalyzed C-N bond formation by allowing for the use of aryl halides containing these functional groups, obviating the need for protecting group manipulations.

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