REACTION OF DIAZONIUM SALTS WITH TRANSITION METALS. I. ARYLATION OF OLEFINS WITH ARENEDIAZONIUM SALTS CATALYZED BY ZERO VALENT PALLADIUM
- 5 February 1977
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 6 (2), 159-162
- https://doi.org/10.1246/cl.1977.159
Abstract
Various olefins, especially those bearing electron donating groups, were successfully arylated by arenediazonium salts in the presence of a catalytic amount of palladium(O) complexes. An arylpalladium species was supposed to be an intermediate in this reaction.Keywords
This publication has 11 references indexed in Scilit:
- Palladium-catalyzed vinyl substitution reactions. I. New synthesis of 2- and 3-phenyl-substituted allylic alcohols, aldehydes, and ketones from allylic alcoholsThe Journal of Organic Chemistry, 1976
- Palladium-catalyzed arylation of allylic alcohols with aryl halidesThe Journal of Organic Chemistry, 1976
- Co-ordination chemistry of aryldiazonium cations: aryldiazenato (arylazo) complexes of transition metals, and the aryldiazenato–nitrosyl analogyChemical Society Reviews, 1975
- Chemistry of dibenzylideneacetone-palladium(0) complexesJournal of Organometallic Chemistry, 1974
- Electronic and steric effects in the olefin arylation and carboalkoxylation reactions with organopalladium compoundsJournal of the American Chemical Society, 1971
- Arylation of Olefin with Aryl Iodide Catalyzed by PalladiumBulletin of the Chemical Society of Japan, 1971
- ALDEHYDES FROM ALLYLIC ALCOHOLS AND PHENYLPALLADIUM ACETATE: 2-METHYL-3-PHENYLPROPIONALDEHYDEOrganic Syntheses, 1971
- Aromatic substitution of olefin—IXTetrahedron, 1969
- Aromatic substitution of olefin—VIIITetrahedron, 1969
- Aromatic substitution of olefin—VIITetrahedron, 1969