Nucleophilic Aromatic Substitution of Hydrogen (PDF)
(Sprache: Englisch)
Nucleophilic aromatic substitution in carbo- and heteroaromatic systems is a subject of considerable interest to chemists. This book uniquely addresses the systematic analysis of a vast range of nucleophilic substitutions of aromatic...
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Nucleophilic aromatic substitution in carbo- and heteroaromatic systems is a subject of considerable interest to chemists. This book uniquely addresses the systematic analysis of a vast range of nucleophilic substitutions of aromatic hydrogen.
- Nucleophilic displacement of hydrogen (the S N/H reactions) in pi-deficient aromatics, such as nitroarenes, arene-metal complexes, and the like
- Nucleophilic displacement of hydrogen in heterocyclic substrates such as pyridines, their aza and benzo analogs, pyrylium and thiapyrylium cations, and other heterocycles
- Mechanisms for the S N/H reactions (S N/H(AE), vicarious nucleophilic substitutions, and radical S N/H substitutions
Autoren-Porträt von Oleg N. Chupakhin, Valery N. Charushin, Henk C. van der Plas
Professor Dr. H.C. van der Plas received his Ph.D. from the University of Amsterdam. He has served the Agricultural University at Wageningen, The Netherlands, from 1966 as a Reader, from 1970 as Professor of Organic Chemistry, and from 1978-1982 and 1989-1995 as Rector Magnificus. His research interest is in chemistry, mainly in the field of nucleophilic substitution and ring transformations. The results of his scientific results are set down in nearly 400 research papers, 20 review articles, and in two monographs, and a book (together with O. Chupakhin and V. Charushin), Nucleophilic Substitution of Aromatic Hydrogen.
Bibliographische Angaben
- Autoren: Oleg N. Chupakhin , Valery N. Charushin , Henk C. van der Plas
- 2012, 367 Seiten, Englisch
- Verlag: Elsevier Science & Techn.
- ISBN-10: 0323140599
- ISBN-13: 9780323140591
- Erscheinungsdatum: 02.12.2012
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Pressezitat
"This is an excellent book that will prove useful for those interested in the chemistry of SN reactions." --JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
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