A new P3N ligand for Pd-catalyzed cross-couplings in water
Erfan Oftadeh1, Max Baumann1, Marco Ortiz1
1Department of Chemistry & Biochemistry, University of California Santa Barbara CA 93106 USA.
Abstract:
A new "P3N" ligand, (n-Bu2N)3P, derived from PCl3 and three equivalents of n-Bu2NH is reported. When complexed to palladium, it readily participates in homogeneous (copper-free) Heck-Cassar-Sonogashira and Suzuki-Miyaura couplings. Reliance on relatively low loadings of Pd is documented under aqueous micellar conditions; i.e., in water containing micelles using the well-established and inexpensive anionic surfactant SDS. Comparisons are shown with several commonly used, representative ligands which, by contrast, are made typically in a number of steps that involve environmentally egregious conditions, and can typically be quite expensive. These issues can now be avoided for these very important reactions using this P3N ligand. Quantum calculations showed the conformational, steric, and electronic nature of P3N ligands and the energetics of their binding to Pd.
More Related Videos
10:12Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols
Published on: April 4, 2014
09:04Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids
Published on: September 21, 2017
Related Concept Videos
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Preparation of Diols and Pinacol Rearrangement
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
Cationic Chain-Growth Polymerization: Mechanism
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F51444.jpg&w=3840&q=50)