Journal ArticleDOI
Palladium/tetraphosphine catalyzed suzuki cross‐coupling of heteroarylboronic acids with aryl halides
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In this paper, the Suzuki reaction of hetero-boronic acids with aryl bromides and also the coupling of arylsboronic acid with heteroaryl bromide was studied.About:
This article is published in Journal of Heterocyclic Chemistry.The article was published on 2008-01-01. It has received 23 citations till now. The article focuses on the topics: Palladium & Aryl.read more
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A new and facile method for the functionalization of a Merrifield resin with terpyridines: application as a heterogeneous catalyst for the synthesis of biaryls in environmentally friendly solvents
Jérôme Husson,Laurent Guyard +1 more
TL;DR: In this article, a Merrifield resin was modified with pendant terpyridine heterocycles in order to develop a new material for heterogeneous catalysis, which relies on the reaction of a pyrrolyl anion with chloromethyl groups present on the resin.
Journal ArticleDOI
Palladium/Tetraphosphine Catalyzed Suzuki Cross‐Coupling of Heteroarylboronic Acids with Aryl Halides.
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Synthesis of 5-membered Heteroaryl-substituted Benzyloxy-benzaldehydes by the Suzuki-Miyaura Coupling Reaction
TL;DR: The Suzuki-Miyaura carbon-carbon cross-coupling reaction was utilized to get five membered heteroaryl-substituted benzyloxy-benzaldehydes as mentioned in this paper .
References
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Journal ArticleDOI
Palladium-catalyzed cross-coupling reactions of organoboron compounds
Norio Miyaura,Akira Suzuki +1 more
TL;DR: In this paper, a cross-coupling reaction is proposed for coupling 1 -Alkenylboron Derivatives: Synthesis of Conjugated Dienes 6.
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Aryl-aryl bond formation by transition-metal-catalyzed direct arylation.
TL;DR: A number of improvements have developed the former process into an industrially very useful and attractive method for the construction of aryl -aryl bonds, but the need still exists for more efficient routes whereby the same outcome is accomplished, but with reduced waste and in fewer steps.
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Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998
TL;DR: The palladium-catalyzed cross-coupling reaction between organoboron compounds and organic halides or triflates provides a powerful and general methodology for the formation of carbon-carbon bonds as discussed by the authors.
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Palladium-Catalyzed Coupling Reactions of Aryl Chlorides
Adam F. Littke,Gregory C. Fu +1 more
TL;DR: This review summarizes both the seminal early work and the exciting recent developments in the area of palladium-catalyzed couplings of aryl chlorides.
Journal ArticleDOI
Catalysts for Suzuki−Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure
TL;DR: Structural studies of various 1.Pd complexes are presented along with computational data that help elucidate the efficacy that 1 imparts on Suzuki-Miyaura coupling processes, and a comparison of the reactions is presented that is informative in determining the relative importance of ligand bulk and electron-donating ability in the high activity of catalysts derived from ligands of this type.