Umlagerung tertiärer Äthinyl-carbinole in ungesättigte Ketone
Kurt H. Meyer,Kurt Schuster +1 more
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This article is published in European Journal of Inorganic Chemistry.The article was published on 1922-04-08 and is currently open access. It has received 176 citations till now.read more
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N-Heterocyclic Carbenes in Late Transition Metal Catalysis
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Homogeneous gold catalysts and alkynes: A successful liaison
TL;DR: The use of homogeneous gold-catalysts and alkynes in organic synthesis is reviewed from its beginnings in C-N-bond formation to the newest developments in C -C-Bond formation in this paper.
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The Meyer–Schuster rearrangement for the synthesis of α,β-unsaturated carbonyl compounds
TL;DR: Recent advances in the Meyer-Schuster reaction are featured, including several demonstrated techniques for improving the scope, andStrengths and weaknesses of each technique are discussed, and outstanding problems that warrant further study are highlighted.
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Progress in the synthesis and transformations of alkylidenecyclopropanes and alkylidenecyclobutanes.
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Olefination of Ketones Using a Gold(III)-Catalyzed Meyer−Schuster Rearrangement
TL;DR: An atom-economical and efficient olefination strategy for ketones is described, which promotes an interaction with the electron-rich acetylenes that catalyzes the Meyer-Schuster rearrangement selectively over other conceivable pathways.