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Titlebook: Catalytic Carbonylation Reactions; Matthias Beller Book 2006 Springer-Verlag Berlin Heidelberg 2006 Organometallic chemistry.Pauson–Khand

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https://doi.org/10.1007/978-3-031-14190-4f oxidative carbonylation is presented, and the generalmechanisms followed by different substrates (alkenes, dienes, allenes, alkynes, ketones, ketenes, aromatichydrocarbons, aliphatic hydrocarbons, alcohols, phenols, amines) leading to a variety of carbonyl compoundsare discussed. The second sectio
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Wilson Kodwo McWilson,Gloria Mensahnd economics by maintaining catalyststability at reduced water concentration. The most significant recent development is the commercialisationby BP Chemicals of the iridium-based Cativa. process. Enhanced stability ofiridium catalysts also allows operation at lower water concentration. Mechanistic s
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1436-6002 ential information on the use of carbon monoxide in organic synthesis. Therefore, the reader will get a balanced view of this developing and complex subject..978-3-642-06955-0978-3-540-33003-5Series ISSN 1436-6002 Series E-ISSN 1616-8534
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Acetic Acid Synthesis by Catalytic Carbonylation of Methanol,nd economics by maintaining catalyststability at reduced water concentration. The most significant recent development is the commercialisationby BP Chemicals of the iridium-based Cativa. process. Enhanced stability ofiridium catalysts also allows operation at lower water concentration. Mechanistic s
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Hydroformylation,d 10 million metric tons annually. Propene-based productsstill account for two-thirds of this volume. Highly selective processes using ligand-modified rhodium catalystshave been developed and are state of the art. Technology and markets for the products have matured, sothere is little room for impro
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