DalPhos Ligands

Professor Mark Stradiotto and coworkers at Dalhousie University have developed air-stable Dalphos, which contains the bulky di(1-adamantyl)phosphino [P(1-Ad)2] fragment. These chelating N,P ligands are useful for previously unprecedented Pd-catalyzed C-N and C-C bond formation. Both Me-DalPhos (Cat. No. 751413) and Mor-DalPhos (Cat. No. 751618) allow for Pd-catalyzed ammonia cross-coupling. In particular, the more reactive Mor-Dalphos improved the scope and utility of ammonia coupling at room temperature.

Cat. No. 759198


Cat. No. 751618


Cat. No. 751413

Benefits of DalPhos Ligands:

  • Monoarylation of ammonia, hydrazine and acetone
  • Air-stable
  • Good functional group tolerance
  • Mild conditions

Me-DalPhos featuring an ortho-dimethylamino group has been shown to be a valuable ligand for the Pd-catalyzed cross-coupling of aryl chlorides and amines (including ammonia). The highly efficient Mor-Dalphos, where the dimethylamino group is replaced by morpholine, easily enables the ammonia coupling of a range of aryl chlorides and aryl tosylates.


Cross-Coupling of Ammonia


Mor-DalPhos can be used for the first Pd-catalyzed cross-coupling of aryl chlorides and tosylates with hydrazine. The Stradiotto group also explored the scope of the reaction of aryl hydrazines with benzaldehydes to afford the corresponding aryl hydrazones.


Cross-Coupling of Hydrazine


The direct arylation of acetone with a range of aryl halides and tosylates has been reported with good monoarylation selectivity. The use of Mor-DalPhos has a key impact on the rate and selectivity of this reaction.


Cross-Coupling of Acetone


The use of Mor-DalPhos for the gold-catalyzed hydroamination of internal aryl alkynes with dialkylamines has been studied. This gold precatalyst featuring a P,N-ligand effects the stereoselective addition of a variety of functionalized dialkylamines to unsymmetrical internal arylacetylenes.


Gold-Catalyzed Hydroamination





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  2.  Lundgren, R. J.; Stradiotto, M. Angew. Chem. Int. Ed. 2010, 49, 8686.
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  4.  Lundgren, R. J.; Sappong-Kumankumah, A.; Stradiotto, M. AChem. Eur. J. 2010, 16, 1983.
  5.  Hesp, K. D.; Stradiotto, M. J. Am. Chem. Soc. 2010, 132, 18026.