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Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity

Ruth Dorel, +1 more
- 09 Sep 2015 - 
- Vol. 115, Iss: 17, pp 9028-9072
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TLDR
Gold(I) complexes selectively activate π-bonds of alkenes in complex molecular settings, which has been attributed to relativistic effects as discussed by the authors, and are the most effective catalysts for the electrophilic activation of alkynes under homogeneous conditions.
Abstract
1.1. General Reactivity of Alkyne-Gold(I) Complexes For centuries, gold had been considered a precious, purely decorative inert metal. It was not until 1986 that Ito and Hayashi described the first application of gold(I) in homogeneous catalysis.1 More than one decade later, the first examples of gold(I) activation of alkynes were reported by Teles2 and Tanaka,3 revealing the potential of gold(I) in organic synthesis. Now, gold(I) complexes are the most effective catalysts for the electrophilic activation of alkynes under homogeneous conditions, and a broad range of versatile synthetic tools have been developed for the construction of carbon–carbon or carbon–heteroatom bonds. Gold(I) complexes selectively activate π-bonds of alkynes in complex molecular settings,4−10 which has been attributed to relativistic effects.11−13 In general, no other electrophilic late transition metal shows the breadth of synthetic applications of homogeneous gold(I) catalysts, although in occasions less Lewis acidic Pt(II) or Ag(I) complexes can be used as an alternative,9,10,14,15 particularly in the context of the activation of alkenes.16,17 Highly electrophilic Ga(III)18−22 and In(III)23,24 salts can also be used as catalysts, although often higher catalyst loadings are required. In general, the nucleophilic Markovnikov attack to η2-[AuL]+-activated alkynes 1 forms trans-alkenyl-gold complexes 2 as intermediates (Scheme 1).4,5a,9,10,12,25−29 This activation mode also occurs in gold-catalyzed cycloisomerizations of 1,n-enynes and in hydroarylation reactions, in which the alkene or the arene act as the nucleophile. Scheme 1 Anti-Nucleophilic Attack to η2-[AuL]+-Activated Alkynes

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References
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Journal ArticleDOI

Gold-Catalyzed Organic Reactions

TL;DR: Important vinylgold intermediates, the transmetalation from gold to other transition metals, the development of new ligands for gold catalysis, and significant contributions from computational chemistry are other crucial points for the field highlighted here.
Journal ArticleDOI

Catalytic Carbophilic Activation: Catalysis by Platinum and Gold π Acids

TL;DR: The ability of platinum and gold catalysts to effect powerful atom-economic transformations has led to a marked increase in their utilization and the application of platinum- and gold-catalyzed transformations in natural product synthesis is discussed.
Journal ArticleDOI

Ligand effects in homogeneous Au catalysis.

TL;DR: The ways in which selectivity can be controlled in homogeneous Au catalysis are enumerated, in the hope that lessons to guide catalyst selection and the design of new catalysts may be distilled from a thorough evaluation of ligand, counterion, and oxidation state effects as they influence chemo-, regio-, and stereoselectivity in homogeneity AuCatalysis.
Journal ArticleDOI

Gold-catalyzed cycloisomerizations of enynes: a mechanistic perspective.

TL;DR: The proposed involvement of cyclopropyl metal carbenes of type 4 in the electrophilic activation of enynes by transition metals was first substantiated in reactions catalyzed by Pd(II), in which the initially formed cycloprostyl palladiumCarbenes undergo [4 + 2] cycloaddition with the double bond of the conjugate enyne.
Journal ArticleDOI

Theoretical chemistry of gold.

TL;DR: The theoretical interpretation of the aurophilic attraction is discussed in detail and a large body of appropriate calculations now exist and their main conclusions are summarized.
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