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Metal‐Catalyzed Reductive Coupling Reactions of Organic Halides with Carbonyl‐Type Compounds

Chemistry - A European Journal · 2014 · Vol. 20(27) · pp. 8242–8258
Toni MoragasArkaitz CorreaRubén Martı́n

Abstract

Metal-catalyzed reductive coupling reactions of aryl halides and (pseudo)halides with carbonyl-type compounds have undergone an impressive development within the last years. These methodologies have shown to be a powerful alternate strategy, practicality aside, to the use of stoichiometric, well-defined, and, in some cases, air-sensitive organometallic species. In this Minireview, the recent findings in this field are summarized, with particular emphasis on the mechanistic interpretation of the results and future aspects of this area of expertise.

Catalytic C–H Functionalization MethodsCatalytic Cross-Coupling ReactionsRadical Photochemical ReactionsHalideArylCatalysisCoupling reactionChemistryAsideStoichiometryMetal carbonylCoupling (piping)Metal

Funding

  • Institut Català d'Investigació Química
  • Ministerio de Ciencia e Innovación
Citations
519
FWCI
14.92
field-weighted impact
References
183
Percentile
100%
vs. same field & year
Citations per year
References
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Accounts of Chemical Research · 2002 · 1,305 citations
Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way
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Reductive Cross‐Coupling Reactions between Two Electrophiles
Chemistry - A European Journal · 2014 · 733 citations
Recent Progress in Nickel‐Catalyzed Biaryl Coupling
European Journal of Organic Chemistry · 2012 · 514 citations
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