Catalysis is a fundamentally sustainable process which can be used to produce a wide range of chemicals and their intermediates. Focussing on those catalytic processes which offer the most sustainability, this book explores recent developments in this field, as well as examining future challenges. The book is divided into four parts, the first two focussing on catalysis through non-endangered metals and the next two catalysis without metals or other endangered elements. Green aspects of the various reactions are also discussed, such as atom economy and use of green solvents and other reaction…mehr
Catalysis is a fundamentally sustainable process which can be used to produce a wide range of chemicals and their intermediates. Focussing on those catalytic processes which offer the most sustainability, this book explores recent developments in this field, as well as examining future challenges. The book is divided into four parts, the first two focussing on catalysis through non-endangered metals and the next two catalysis without metals or other endangered elements. Green aspects of the various reactions are also discussed, such as atom economy and use of green solvents and other reaction conditions. Together these four volumes examine the progress in sustainable catalysis in all areas of chemistry, and are an important reference for researchers working in catalysis and green chemistry.
Michael North holds the Chair in Green Chemistry at the University of York. He is also Joint Chair of the CO2Chem, an EPSCR-supported Grand Challenge Network examining CO2 chemistry. His research interests are in green organic chemistry, especially sustainable catalysis and the utilization of sustainable feedstocks including CO2.
Inhaltsangabe
Volume 1: Introduction Alkali metal (Li, Na, K)-based Catalysts Magnesium and Calcium-based Catalysts Scandium and Yttrium-based Catalysts Titanium-based Catalysts for Non-asymmetric Synthesis of Small Molecules Titanium-based Catalysts for Polymer Synthesis Titanium-based Catalysts for Asymmetric Transformations Zirconium-based Catalysts Vanadium and Niobium-based Catalysts Chromium-based Catalysts Manganese-based Catalysts Metallic Iron, Iron Oxides and Iron Salt-based Catalysts Iron Complex-based Catalysts Nickel-based Catalysts Copper-based Catalysts Gold-based Catalysts Cadmium-based Catalysts Aluminium-based Catalysts for Non-asymmetric Transformations Aluminium-based Catalysts for Asymmetric Transformations Thallium-based Catalysts Tin-based Catalysts Lead-based Catalysts Index Volume 2: Introduction Base Catalysis in Non-asymmetric Synthesis Homogeneous Acid Catalysis in Non-asymmetric Synthesis Heterogeneous Acid Catalysis in Non-asymmetric Synthesis Proline as an Asymmetric Organocatalyst Prolinamides as Asymmetric Organocatalysts Prolinols and their Carbon Ethers as Asymmetric Organocatalysts Prolinol Silyl Ethers as Asymmetric Organocatalysts Other 2-substituted Pyrrolidines as Asymmetric Organocatalysts Hydroxyproline Derivatives as Asymmetric Organocatalysts Other Substituted Pyrrolidines as Asymmetric Organocatalysts Other Amino Acids as Asymmetric Organocatalysts Peptides as Asymmetric Organocatalysts Non-quaternized Cinchona Alkaloid Derivatives as Asymmetric Organocatalysts for Carbon-Carbon Bond Forming Reactions Non-quaternized Cinchona Alkaloid Derivatives as Asymmetric Organocatalysts for Carbon-Heteratom Bond Forming Reactions Cinchona Alkaloid Derivatives as Asymmetric Phase Transfer Catalysts Binaphthyl-Derived Cyclic Amines and their Salts as Asymmetric Organocatalysts Imidazolidinones as Asymmetric Organocatalysts Ureas and Thioureas as Asymmetric Organocatalysts N-heterocyclic Carbenes as Asymmetric Organocatalysts Lewis-base Asymmetric Organocatalysts Chiral Imidazoles and Pyridines as Asymmetric Organocatalysts Chiral Guanines as Asymmetric Organocatalysts Alcohols, Phenols and Carboxylic Acids as Asymmetric Organocatalysts Index
Volume 1: Introduction Alkali metal (Li, Na, K)-based Catalysts Magnesium and Calcium-based Catalysts Scandium and Yttrium-based Catalysts Titanium-based Catalysts for Non-asymmetric Synthesis of Small Molecules Titanium-based Catalysts for Polymer Synthesis Titanium-based Catalysts for Asymmetric Transformations Zirconium-based Catalysts Vanadium and Niobium-based Catalysts Chromium-based Catalysts Manganese-based Catalysts Metallic Iron, Iron Oxides and Iron Salt-based Catalysts Iron Complex-based Catalysts Nickel-based Catalysts Copper-based Catalysts Gold-based Catalysts Cadmium-based Catalysts Aluminium-based Catalysts for Non-asymmetric Transformations Aluminium-based Catalysts for Asymmetric Transformations Thallium-based Catalysts Tin-based Catalysts Lead-based Catalysts Index Volume 2: Introduction Base Catalysis in Non-asymmetric Synthesis Homogeneous Acid Catalysis in Non-asymmetric Synthesis Heterogeneous Acid Catalysis in Non-asymmetric Synthesis Proline as an Asymmetric Organocatalyst Prolinamides as Asymmetric Organocatalysts Prolinols and their Carbon Ethers as Asymmetric Organocatalysts Prolinol Silyl Ethers as Asymmetric Organocatalysts Other 2-substituted Pyrrolidines as Asymmetric Organocatalysts Hydroxyproline Derivatives as Asymmetric Organocatalysts Other Substituted Pyrrolidines as Asymmetric Organocatalysts Other Amino Acids as Asymmetric Organocatalysts Peptides as Asymmetric Organocatalysts Non-quaternized Cinchona Alkaloid Derivatives as Asymmetric Organocatalysts for Carbon-Carbon Bond Forming Reactions Non-quaternized Cinchona Alkaloid Derivatives as Asymmetric Organocatalysts for Carbon-Heteratom Bond Forming Reactions Cinchona Alkaloid Derivatives as Asymmetric Phase Transfer Catalysts Binaphthyl-Derived Cyclic Amines and their Salts as Asymmetric Organocatalysts Imidazolidinones as Asymmetric Organocatalysts Ureas and Thioureas as Asymmetric Organocatalysts N-heterocyclic Carbenes as Asymmetric Organocatalysts Lewis-base Asymmetric Organocatalysts Chiral Imidazoles and Pyridines as Asymmetric Organocatalysts Chiral Guanines as Asymmetric Organocatalysts Alcohols, Phenols and Carboxylic Acids as Asymmetric Organocatalysts Index
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