Issue Date: September 7, 2015
A Little Palladium Does A Lot Of Cross-Coupling
As part of their efforts in developing greener chemistry, Bruce H. Lipshutz and his group at the University of California, Santa Barbara, have already pared Suzuki-Miyaura cross-coupling reactions down to no organic solvent, little if any heating, and a minimum of palladium catalyst. But the fact that their recyclable aqueous reaction system still requires a relatively expensive amount of scarce palladium has bothered Lipshutz. His group has now found a way . . .
To view the rest of this content, please log in with your ACS ID.
- Chemical & Engineering News
- ISSN 0009-2347
- Copyright © American Chemical Society