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Open AccessJournal ArticleDOI

Oxidative Coupling of Aromatic Substrates with Alkynes and Alkenes under Rhodium Catalysis

Tetsuya Satoh, +1 more
- 04 Oct 2010 - 
- Vol. 16, Iss: 37, pp 11212-11222
TLDR
Aromatic substrates with oxygen- and nitrogen-containing substituents undergo oxidative coupling with alkynes and alkenes under rhodium catalysis through regioselective C-H bond cleavage, creating fused-ring systems through these reactions.
Abstract
Aromatic substrates with oxygen- and nitrogen-containing substituents undergo oxidative coupling with alkynes and alkenes under rhodium catalysis through regioselective C-H bond cleavage. Coordination of the substituents to the rhodium center is the key to activate the C-H bonds effectively. Various fused-ring systems can be constructed through these reactions.

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Citations
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Journal ArticleDOI

Carboxylate-assisted transition-metal-catalyzed C-H bond functionalizations: mechanism and scope.

TL;DR: This review summarizes the development and scope of carboxylates as cocatalysts in transition-metal-catalyzed C-H functionalizations until autumn 2010 and proposes new acronyms, such as CMD (concerted metalationdeprotonation), IES (internal electrophilic substitution), or AMLA (ambiphilic metal ligand activation), which describe related mechanisms.
Journal ArticleDOI

C–C, C–O and C–N bond formation via rhodium(III)-catalyzed oxidative C–H activation

TL;DR: The facile construction of C-E (E = C, N, S, or O) bonds makes Rh(III) catalysis an attractive step-economic approach to value-added molecules from readily available starting materials.
Journal ArticleDOI

Beyond directing groups: transition-metal-catalyzed C-H activation of simple arenes.

TL;DR: In this review, recent advances in the emerging field of non-chelate-assisted C-H activation are discussed, highlighting some of the most intriguing and inspiring examples of induction of reactivity and selectivity.
Journal ArticleDOI

3d Transition Metals for C-H Activation.

TL;DR: A comprehensive overview on first row transition metal catalysts for C-H activation until summer 2018 is provided.
References
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Journal ArticleDOI

Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.

TL;DR: A review of palladium-catalyzed coupling of CH bonds with organometallic reagents through a PdII/Pd0 catalytic cycle can be found in this paper.
Journal ArticleDOI

Rhodium-Catalyzed C-C Bond Formation via Heteroatom-Directed C-H Bond Activation

TL;DR: This review focuses on Rh-catalyzed methods for C-H bond functionalization, which have seen widespread success over the course of the last decade and are discussed in detail in the accompanying articles in this special issue of Chemical Reviews.
Journal ArticleDOI

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.
Journal ArticleDOI

Activation of c-h bonds by metal complexes

TL;DR: In this article, it was shown that the same alkylhydridoplatinum(IV) complex is the intermediate in the reaction of ethane with platinum(II) σ-complexes.
Journal ArticleDOI

Palladium- and Copper-Catalyzed Arylation of Carbon-Hydrogen Bonds

TL;DR: A general method for directing-group-containing arene arylation by aryl iodides is developed and palladium acetate as the catalyst, which arylated anilides, benzamides, benzoic acids, benzylamines, and 2-substituted pyridine derivatives under nearly identical conditions.
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