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Palladium-Catalyzed Selective Generation of CO from Formic Acid for Carbonylation of Alkenes.
Sang, Rui; Kucmierczyk, Peter; Dong, Kaiwu; Franke, Robert; Neumann, Helfried; Jackstell, Ralf; Beller, Matthias.
Afiliação
  • Sang R; Leibniz-Institut für Katalyse e.V. an der Universität Rostock , Albert-Einstein-Straße 29a , Rostock 18059 , Germany.
  • Kucmierczyk P; Leibniz-Institut für Katalyse e.V. an der Universität Rostock , Albert-Einstein-Straße 29a , Rostock 18059 , Germany.
  • Dong K; Lehrstuhl für Theoretische Chemie , Ruhr-Universität Bochum , 44780 Bochum , Germany.
  • Franke R; Leibniz-Institut für Katalyse e.V. an der Universität Rostock , Albert-Einstein-Straße 29a , Rostock 18059 , Germany.
  • Neumann H; Lehrstuhl für Theoretische Chemie , Ruhr-Universität Bochum , 44780 Bochum , Germany.
  • Jackstell R; Evonik Performance Materials GmbH , Paul-Baumann-Straße 1 , 45772 Marl , Germany.
  • Beller M; Leibniz-Institut für Katalyse e.V. an der Universität Rostock , Albert-Einstein-Straße 29a , Rostock 18059 , Germany.
J Am Chem Soc ; 140(15): 5217-5223, 2018 04 18.
Article em En | MEDLINE | ID: mdl-29528637
ABSTRACT
A general and selective palladium-catalyzed alkoxycarbonylation of all kinds of alkenes with formic acid (HCOOH, FA) is described. Terminal, di-, tri-, and tetra-substituted including functionalized olefins are converted into linear esters with high yields and regioselectivity. Key-to-success is the use of specific palladium catalysts containing ligands with built-in base, e.g., L5. Comparison experiments demonstrate that the active catalyst system not only facilitates isomerization and carbonylation of alkenes but also promotes the selective decomposition of HCOOH to CO under mild conditions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article