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Journal ArticleDOI

Efficient Copper(I)-Catalyzed C–S Cross Coupling of Thiols with Aryl Halides in Water

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TLDR
In this paper, the C-S cross coupling of thiols with aryl halides in the presence of tetrabutylammonium bromide in water was investigated.
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This article is published in European Journal of Organic Chemistry.The article was published on 2008-02-01. It has received 134 citations till now. The article focuses on the topics: Aryl.

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Copper catalysed Ullmann type chemistry: From mechanistic aspects to modern development

TL;DR: The history and development of coupling reactions between aryl halides and various classes of nucleophiles is discussed, focusing mostly on the different mechanisms proposed through the years.
Journal ArticleDOI

Catalytic Organic Reactions in Water toward Sustainable Society

TL;DR: This Review addresses advances over the past decade in catalytic reactions using water as a reaction medium by addressing the development of water-compatible catalysts and heterogeneous catalysts.
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CuO nanoparticles catalyzed C-N, C-O, and C-S cross-coupling reactions: scope and mechanism.

TL;DR: CuO nanoparticles have been studied for C-N, C-O, and C-S bond formations via cross-coupling reactions of nitrogen, oxygen, and sulfur nucleophiles with aryl halides in the presence of a base such as KOH, Cs(2)CO(3), and K(2]CO( 3) at moderate temperature.
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The mechanism of the modified Ullmann reaction

TL;DR: A recent DFT study by Houk, Buchwald and co-workers shows that the modified Ullmann reaction between aryl iodide and amines or primary alcohols proceeds either via an SET or an IAT mechanism, suggesting a Cu(I)/Cu(III) type mechanism for the amidation (Goldberg) reaction.
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Modern Synthetic Methods for Copper‐Mediated C(aryl) ? O, C(aryl) ? N, and C(aryl) ? S Bond Formation

TL;DR: In this article, the authors highlight the recent developments in the copper-mediated (both stoichiometric and catalytic) reactions of aryl boronic acids as reaction partners in both O- and N-arylation.
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Transition Metal Catalyzed Synthesis of Arylamines and Aryl Ethers from Aryl Halides and Triflates: Scope and Mechanism.

TL;DR: Oxidative addition and reductive elimination are the central steps in new palladium-catalyzed chemistry that forms C-N and C-O bonds in arylamines and ethers.
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