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Volume 94 Issue 10 | p. 10 | News of The Week
Issue Date: March 7, 2016 | Web Date: March 3, 2016

Phosphine ligand provides a new low for palladium catalysis

Sterically encumbered oxophosphole enables cross-coupling of complex aryl partners in water with a minimal amount of catalyst
Department: Science & Technology
News Channels: Environmental SCENE, Organic SCENE
Keywords: green chemistry, cross-coupling, nanoreactor, HandaPhos, phosphine ligand, palladium

Palladium is the undisputed champion when it comes to catalyst metals, enabling chemists to carry out a versatile array of cross-coupling reactions. Bruce H. Lipshutz and his group at the University of California, Santa Barbara, have a goal to take this versatility further by seeing how green and efficient they can make palladium catalysis.

In their latest endeavor, the Lipshutz group and its collaborators . . .

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