{ALD} Beilstein: 16,III,835

{PUB} Crystallography Open Database (COD)|PubChem --- Bulky triarylarsines are effective ligands for palladium catalysed Heck olefination. --- https://pubmed.ncbi.nlm.nih.gov/15824787

{ALF} Preferred phosphine ligand for use in combination with Pd salts in the Heck-type coupling reactions of vinylic halides. For examples, see Palladium(II)­ acetate, 10516. For a review of the Heck reaction, see: Org. React., 27, 345 (1982).

{PUB} PubChem --- Palladium-Catalyzed Cross-Coupling of Sterically Demanding Boronic Acids with α-Bromocarbonyl Compounds --- https://pubmed.ncbi.nlm.nih.gov/21863787

{PUB} PubChem --- Palladium-Catalyzed Intramolecular Coupling between Aryl Iodides and Allyl Moieties via Thermal and Microwave-Assisted Conditions --- https://pubmed.ncbi.nlm.nih.gov/15631454

{PUB} PubChem --- Palladium‐Catalyzed Intramolecular C(sp3)H Functionalization: Catalyst Development and Synthetic Applications --- https://pubmed.ncbi.nlm.nih.gov/17044108

{PUB} PubChem --- Remarkable effect of phosphine on the reactivity of O,P-acetal--efficient substitution reaction of O,P-acetal --- https://pubmed.ncbi.nlm.nih.gov/20449525

{PUB} PubChem --- Synthesis of InP nanofibers from tri(m-tolyl)phosphine: an alternative route to metal phosphide nanostructures --- https://pubmed.ncbi.nlm.nih.gov/20023954

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{PUB} PubChem|Springer Nature --- Stereoselective synthesis of (+/-)-epibatidine analog:(+/-)-2beta-(2-chloro-5-pyridinyl)-8-azabicyclo[3.2.1] octane --- https://pubmed.ncbi.nlm.nih.gov/10403134

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