{PUB} Springer Nature --- 1.2.15 Rhodium Rh --- https://doi.org/10.1007/10201323_49

{PUB} Springer Nature --- Direct and selective hydrogenolysis of arenols and aryl methyl ethers --- https://pubmed.ncbi.nlm.nih.gov/25704229

{PUB} Springer Nature --- Mechanistic Considerations in the Development and Use of Azine, Diazine and Azole N-Oxides in Palladium-Catalyzed Direct Arylation --- https://doi.org/10.1007/128_2009_14

{PUB} Thieme Chemistry --- 1,2-Disubstituted E-Alkenes via β-Monosubstituted E-Alkenyl Derivatives --- https://science-of-synthesis.thieme.com/app/text/?id=SD-047-00405

{PUB} Thieme Chemistry --- Couplings of Alkyl Boron Compounds (Suzuki–Miyaura Reaction) Mediated by Palladium and Nickel --- https://science-of-synthesis.thieme.com/app/text/?id=SD-048-00019

{PUB} Thieme Chemistry --- Dienyl Phosphine Complexes by Substitution --- https://science-of-synthesis.thieme.com/app/text/?id=SD-001-00560

{PUB} Thieme Chemistry --- From Alkyldihalophosphines and Organometallic Alkali Metal Compounds or Grignard Reagents --- https://science-of-synthesis.thieme.com/app/text/?id=SD-042-00087

{PUB} Thieme Chemistry --- From Dialkylhalophosphines and Organometallic Alkali Metal Compounds or Grignard Reagents --- https://science-of-synthesis.thieme.com/app/text/?id=SD-042-00088

{PUB} Thieme Chemistry --- Hiyama Cross-Coupling Reaction --- https://science-of-synthesis.thieme.com/app/text/?id=SD-045-00570

{PUB} Thieme Chemistry --- In the Presence of Directing Groups --- https://science-of-synthesis.thieme.com/app/text/?id=SD-045-00553

{PUB} Thieme Chemistry --- Metal-Catalyzed Cross-Coupling Reactions --- https://science-of-synthesis.thieme.com/app/text/?id=SD-106-00027

{PUB} Thieme Chemistry --- Palladium-Promoted Cross-Coupling Reactions --- https://science-of-synthesis.thieme.com/app/text/?id=SD-042-00430

{PUB} Thieme Chemistry --- Preparation of Aryl(dicyclohexyl)phosphines by C–P Bond-Forming Cross-Coupling in Water Catalyzed by an Amphiphilic-Resin-Sup