NaOH-Promoted cross-coupling reactions of organosilicon compounds with organic halides: Practical routes to biaryls, alkenylarenes and conjugated dienes
- 20 January 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (3) , 439-442
- https://doi.org/10.1016/s0040-4039(96)02320-9
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Cross-Coupling Reactions of Aryl Chlorides with Organochlorosilanes: Highly Effective Methods for Arylation or Alkenylation of Aryl ChloridesThe Journal of Organic Chemistry, 1996
- Regio- and Stereochemical Aspects of the Palladium-Catalyzed Reactions of SilanesChemical Reviews, 1995
- Transformations of Chloroarenes, Catalyzed by Transition-Metal ComplexesChemical Reviews, 1994
- Reactivity of penta- and hexacoordinate silicon compounds and their role as reaction intermediatesChemical Reviews, 1993
- Mechanism of aryl chloride oxidative addition to chelated palladium(0) complexesOrganometallics, 1993
- In aqua synthesis of water-soluble poly(p-phenylene) derivativesJournal of the American Chemical Society, 1991
- Chlorocarbon Activation: Catalytic Carbonylation of Dichloromethane and ChlorobenzeneAngewandte Chemie International Edition in English, 1989
- Palladium catalysed cross-coupling reactions with difunctional tin reagents: a general route to aromatic polymersJournal of the Chemical Society, Chemical Communications, 1989
- Alkenylfluorosilanes as widely applicable substrates for the palladium-catalyzed coupling of alkenylsilane/fluoride reagents with alkenyl iodidesThe Journal of Organic Chemistry, 1989
- Synthesis of Ketone Derivatives of Biphenyl by the Friedel-Crafts Reaction1Journal of the American Chemical Society, 1941