New Efficient Nickel- and Palladium-Catalyzed Cross-Coupling Reactions Mediated by Tetrabutylammonium Iodide
- 2 October 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 1 (9) , 1323-1326
- https://doi.org/10.1021/ol9907872
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Homocoupling of Aryl Halides Promoted by Tetrabutylammonium FluorideSynlett, 1999
- Ni(II)-Catalyzed Cross-Coupling between Polyfunctional Arylzinc Derivatives and Primary Alkyl IodidesJournal of the American Chemical Society, 1998
- Cross-Coupling Reaction of Organostannanes with Aryl Halides Catalyzed by Nickel-Triphenylphosphine or Nickel-Lithium Halide ComplexSynthesis, 1998
- Highly Stereo- and Chemoselective Iron-Catalyzed Alkenylation of Organomagnesium CompoundsSynthesis, 1998
- Nickel(0)-catalyzed cross coupling of aryl O-carbamates and aryl triflates with Grignard reagents. Directed ortho metalation-aligned synthetic methods for polysubstituted aromatics via a 1,2-dipole equivalentThe Journal of Organic Chemistry, 1992
- New synthetic applications of the dithioacetal functionalityAccounts of Chemical Research, 1991
- Preparation and reactions of functionalized benzylic organometallics of zinc and copperOrganometallics, 1990
- Palladium- or nickel-catalyzed cross coupling. A new selective method for carbon-carbon bond formationAccounts of Chemical Research, 1982
- Palladium-catalyzed cross-coupling reaction of homoallylic or homopropargylic organozincs with alkenyl halides as a new selective route to 1,5-dienes and 1,5-enynesJournal of the American Chemical Society, 1980
- Nickel and palladium complex catalyzed cross-coupling reactions of organometallic reagents with organic halidesPure and Applied Chemistry, 1980