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Side Reactions in Organic Synthesis II – Aromatic Substitutions

Software / Digital Media
312 Seiten
2014
Wiley-VCH Verlag GmbH (Hersteller)
978-3-527-68780-0 (ISBN)
CHF 146,95 inkl. MwSt
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This new textbook is the successor to the volume "Side Reactions in Organic Synthesis - A Guide to Successful Synthesis Design" (2004), written by the same author. Whereas the predecessor mainly covered the limitations of aliphatic substitution reactions, this new volume focuses on the most important aromatic substitution reactions, both electrophilic and nucleophilic, such as amination reactions, halogenation reactions, Friedel-Crafts acylations, or transition metal-catalyzed arylation reactions. Each chapter not only describes the scope of a specific reaction type, but also reveals what cannot be achieved with this reaction, i.e. what type of side reactions are to be expected with certain starting materials or electrophiles/nucleophiles. With its unique approach, this is a must-have book for graduate students in organic chemistry and synthetic chemists both in academia and industry!

Florencio Zaragoza Dorwald studied chemistry at the Georg-August University in Gottingen, Germany, and Universite Louis Pasteur, Strasbourg, France, where he obtained his Ph.D. in 1990 on the synthesis of natural products under the guidance of M. Franck-Neumann and M. Miesch. He spent one postdoctoral year in both the groups of A. Pfaltz (University of Basel) and A. P. Marchand (University of North Texas), and then worked on the synthesis of unnatural amino acids at the Technical University of Dresden. From 1994 to 2007 he had a position as a medicinal chemist at Novo Nordisk A/S, Denmark. Currently, he is employed as organic chemist at Lonza AG in Visp, Switzerland.

Erscheint lt. Verlag 30.5.2014
Verlagsort Weinheim
Sprache englisch
Maße 244 x 170 mm
Gewicht 666 g
Themenwelt Naturwissenschaften Chemie Organische Chemie
Naturwissenschaften Chemie Physikalische Chemie
ISBN-10 3-527-68780-7 / 3527687807
ISBN-13 978-3-527-68780-0 / 9783527687800
Zustand Neuware
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