Resorcinarene‐Based o‐Biarylphosphines in Palladium‐Catalysed Suzuki–Miyaura Cross‐Coupling Reactions of Bulky Substrates - Elaieb - 2017 - European Journal of Inorganic Chemistry - Wiley Online Library
Dichlorobis(tri-o-tolylphosphine)palladium(II) 97 % | 40691-33-6 | Sigma-Aldrich
Tri(o-tolyl)phosphine 97 % | 6163-58-2 | Sigma-Aldrich
Convenient and General Palladium‐Catalyzed Carbonylative Sonogashira Coupling of Aryl Amines - Wu - 2011 - Angewandte Chemie International Edition - Wiley Online Library
Tri(2-furyl)phosphine 99 % | 5518-52-5 | Sigma-Aldrich
References
Nano-palladium is a cellular catalyst for in vivo chemistry. - Nat. Commun. - X-MOL
Carbonylation of terminal alkynes catalysed by Pd complexes in combination with tri(2-furyl)phosphine and methanesulfonic acid - ScienceDirect
Tri(2-furyl)phosphine 99 % | 5518-52-5 | Sigma-Aldrich
Resorcinarene‐Based o‐Biarylphosphines in Palladium‐Catalysed Suzuki–Miyaura Cross‐Coupling Reactions of Bulky Substrates - Elaieb - 2017 - European Journal of Inorganic Chemistry - Wiley Online Library
Construction of axial chirality via palladium/chiral norbornene cooperative catalysis | Nature Catalysis
TRI(2-FURYL)PHOSPHINE | 5518-52-5
Bis(1,10-phenanthroline)palladium(II) Bis(hexafluorophosphate) 113173-22-1 | TCI EUROPE N.V.
Determination of the Half-Reaction Time | Download Scientific Diagram
References
China Tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)4) CAS No.: 14221-01-3 Manufacturers - Free Sample - Alfa Chemical
Dichlorobis(tri-o-tolylphosphine)palladium(II) 97 % | 40691-33-6 | Sigma-Aldrich
Tri(o-tolyl)phosphine for highly efficient Suzuki coupling of propargylic carbonates with boronic acids - Chemical Communications (RSC Publishing)
Synthesis of diaryl ketonesvia a phosphine-free Fukuyama reaction - Chemical Communications (RSC Publishing)
Tri-(2-furyl)phosphine, 98%, ACROS Organics | Fisher Scientific
Carbonylation of terminal alkynes catalysed by Pd complexes in combination with tri(2-furyl)phosphine and methanesulfonic acid - ScienceDirect
![Phosphine Ligands [Cross-coupling Reaction using Transition Metal Catalysts] | TCI AMERICA](https://www.tcichemicals.com/medias/T1643.jpg?context=bWFzdGVyfHJvb3R8Mzk2MTR8aW1hZ2UvanBlZ3xoZGMvaDA5Lzg5MzI0ODgyNDkzNzQvVDE2NDMuanBnfDFiZTAzOWNlZGFiNjZjZDMwYzZjZGIzNzY4MWVhMGVkZGEzNTRjMzg0YmVjNDYwNTNlYzk5MzEwOGIyN2EwMDM "Phosphine Ligands [Cross-coupling Reaction using Transition Metal Catalysts] | TCI AMERICA")
Phosphine Ligands [Cross-coupling Reaction using Transition Metal Catalysts] | TCI AMERICA
Cationic palladium(II)–acetylacetonate complexes containing phosphine and aminophosphine ligands and their catalytic activities in telomerization of 1,3-butadiene with methanol - ScienceDirect
