Palladium-catalyzed arylation of polar organometallics mediated by 9-methoxy-9-borabicyclo[3.3.1]nonane: Suzuki reactions of extended scope
- 1 October 1995
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 51 (41) , 11165-11176
- https://doi.org/10.1016/0040-4020(95)00677-z
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Suzuki-type cross coupling reactions using palladium-water soluble catalyst. Synthesis of functionalized dienesTetrahedron Letters, 1995
- Scope and Limitations of the Palladium-Catalyzed Cross-Coupling Reaction of in situ Generated Organoboranes with Aryl and Vinyl HalidesThe Journal of Organic Chemistry, 1994
- Highly Efficient and Accelerated Suzuki Aryl Couplings Mediated by Phosphine-Free Palladium SourcesThe Journal of Organic Chemistry, 1994
- Aryl couplings with heterogeneous palladium catalystsTetrahedron Letters, 1994
- New synthetic transformations via organoboron compoundsPure and Applied Chemistry, 1994
- Combined directed ortho metalation-cross coupling strategies. Design for natural product synthesisPublished by Walter de Gruyter GmbH ,1994
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboronic Acids with Organic Electrophiles.Acta Chemica Scandinavica, 1993
- Synthetic studies via the cross-coupling reaction of organoboron derivatives with organic halidesPure and Applied Chemistry, 1991
- Novel and convenient method for the stereo- and regiospecific synthesis of conjugated alkadienes and alkenynes via the palladium-catalyzed cross-coupling reaction of 1-alkenylboranes with bromoalkenes and bromoalkynesJournal of the American Chemical Society, 1985
- Organoboron compounds in new synthetic reactionsPure and Applied Chemistry, 1985