Bio-inspired Catalysts

With the aim of complementing well-established catalytic strategies for enantioselective catalysis, the field of artificial metalloenzymes has attracted increasing interest in the past decade. Artificial metalloenzymes result from the incorporation of a catalytically active organometallic moiety wit...

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Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Ward, Thomas R. (Editor)
Format: Electronic
Language:English
Published: Berlin, Heidelberg : Springer Berlin Heidelberg, 2009.
Series:Topics in Organometallic Chemistry, 25
Subjects:
Online Access:https://ezaccess.library.uitm.edu.my/login?url=http://dx.doi.org/10.1007/978-3-540-87757-8
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505 0 # |a E.W. Dijk, G. Roelfes, and B.L. Feringa: DNA in Metal Catalysis -- S. Abe, T. Ueno, and Y. Watanabe: Artificial Metalloproteins exploiting vacant Space: Preparation, Structures, and Functions -- Q. Jing, K. Okrasa, and R. Kazlauskas: Manganese-Substituted-a-Carbonic Anhydrase as an Enantioselective Peroxidase -- M.T. Reetz: Directed Evolution of Stereoselective Hybrid Catalysts -- T.R. Ward: Artificial Metalloenzymes for Enantioselective Catalysis based on the Biotin-Avidin Technology.-. 
520 # # |a With the aim of complementing well-established catalytic strategies for enantioselective catalysis, the field of artificial metalloenzymes has attracted increasing interest in the past decade. Artificial metalloenzymes result from the incorporation of a catalytically active organometallic moiety within a macromolecular host. Localization of the competent metal is ensured either by covalent, dative or supramolecular anchoring in either DNA or a protein scaffold. The properties of the resulting hybrid catalysts combine attractive features of both homogeneous and enzymatic catalysis. In particular, the optimization of such systems can be achieved both by chemical and genetic means. The book, consisting of five chapters written by leading experts, critically summarizes the state of the art in enantioselective epoxidation, sulfoxidation, fluorination, hydrogenation, allylic alkylation, Diels-Alder cycloadditions as well as Michael additions catalyzed by artificial metalloenzymes. This timely review unambiguously demonstrates the compatibility and complementarity of organometallic and enzymatic catalysis. 
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