The Claisen Rearrangement
Methods and Applications

1. Auflage Februar 2007
XIX, 572 Seiten, Hardcover
739 Abbildungen
51 Tabellen
Handbuch/Nachschlagewerk
Kurzbeschreibung
The first comprehensive coverage of all facets of this elegant reaction type, helping every organic chemist to find the best solution for any claisen rearrangement problem.
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The first comprehensive coverage of all facets of the Claisen rearrangement and its variants. As such, this book helps synthetic chemists to exploit the vast potential of this elegant C-C linking reaction, discusses a wealth of catalytic options, and gives those more theory-minded chemists a detailed insight into the mechanistic aspects of the Claisen rearrangement. An invaluable source of information and a ready reference for all organic and catalytic chemists, as well as those working with/on organometallics, and in industry.
Theoretical Aspects of the Claisen Rearrangement
Chorismate Mutase-Catalyzed Claisen Rearrangement
Chiral Metal Complex-Catalyzed Aliphatic Claisen Rearrangement
Alphabetic and Aromatic Claisen Rearrangement
Metal-Catalyzed Claisen Rearrangement
Simple Enolate and Chelate Enolate Claisen Rearrangement
Claisen-Johnson Orthoester Rearrangement
The Meerwein-Eschenmoser Claisen Rearrangement
The Carroll Rearrangement
Thio-Claisen Rearrangement
Aza-Claisen Rearrangement
Angewandte Chemie, 10/2007
Udo Nubbemeyer received his Diploma and PhD in the group of Prof. Dr. E. Winterfeldt (University of Hannover) and spent a postdoctoral spell at the Ciba-Geigy Laboratory at the University of Fribourg (Switzerland) with Prof. D. Bellus and Dr. B. Ernst (1989/1990). From 1991 to 1996, he worked on his 'Habilitation' in the group of Prof. Dr. J. Mulzer (Freie Universität Berlin). Then, he passed an assistant lecturer period in Berlin and a temporary professorship at the TU Dresden (1999/2001). Actually, he works as an associate professor at the Johannes Gutenberg-Universität of Mainz. His major topics of interest are olefin synthesis, aza Claisen rearrangements, radical cyclizations, medium-sized rings, total synthesis of natural and pharmaceutically important products, alkaloids, eicosanoids, steroids, and amino acids.