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Applied cross-coupling reactions / / Yasushi Nishihara, editor



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Titolo: Applied cross-coupling reactions / / Yasushi Nishihara, editor Visualizza cluster
Pubblicazione: New York, : Springer, 2013
Edizione: 1st ed. 2013.
Descrizione fisica: 1 online resource (245 p.)
Disciplina: 547
Soggetto topico: Organic compounds - Synthesis
Metal catalysts
Altri autori: NishiharaYasushi  
Note generali: Description based upon print version of record.
Nota di bibliografia: Includes bibliographical references and index.
Nota di contenuto: pt. I. Metal-catalyzed cross-coupling reactions -- pt. II. Applications of the cross-coupling reactions -- pt. III. Recent advances in cross-coupling reactions.
Sommario/riassunto: “Applied Cross-Coupling Reactions” provides students and teachers of advanced organic chemistry with an overview of the history, mechanisms and applications of cross-coupling reactions. Since the discovery of the transition-metal-catalyzed cross-coupling reactions in 1972, numerous synthetic uses and industrial applications have been developed. The mechanistic studies of the cross-coupling reactions have disclosed that three fundamental reactions: oxidative addition, transmetalation, and reductive elimination, are involved in a catalytic cycle. Cross-coupling reactions have allowed us to produce a variety of compounds in industrial areas, such as natural products, pharmaceuticals, liquid crystals and conjugate polymers for use in electronic devices. Indeed, the Nobel Prize for Chemistry 2010 was awarded for work on cross-coupling reactions In this book, the recent trends of cross-coupling reactions are also introduced from the viewpoint of designing the synthesis, and catalytic activities of the transition-metal catalysts.
Titolo autorizzato: Applied cross-coupling reactions  Visualizza cluster
ISBN: 1-283-93512-0
3-642-32368-5
Formato: Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione: Inglese
Record Nr.: 9910155334603321
Lo trovi qui: Univ. Federico II
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Serie: Lecture notes in chemistry ; ; 80.