Fr. 224.00

Asymmetric Organic Synthesis with Enzymes

Inglese · Copertina rigida

Spedizione di solito entro 1 a 3 settimane (non disponibile a breve termine)

Descrizione

Ulteriori informazioni

Perfect for biochemists, synthetic and organic chemists, this book covers all important reactions, including C-C coupling reactions, oxidation reactions and many more.Divided into two parts, the first section on methodology presents new innovative methods for enzymatic catalysis optimization, including such new trends as medium engineering, directed evolution and computer-aided prediction of enantioselectivity. The second and main section deals with applications to synthesis, showing important reaction types and their applications. Only those reactions with very high selectivity are presented, allowing readers to improve their own reaction yields.

Sommario

METHODOLOGYMedium Engineering:Directed evolution:The search for new enzymes:SYNTHETIC APPLICATIONSDynamic Kinetic Resolutions:Deracemization and Enantioconvergent Processes:Transesterification and hydrolysis of carboxylic acid derivatives, alcohols and epoxidesAminolysis and ammonolysis of carboxylic acid derivatives:Reduction Reactions:Oxidation Reactions:Making and breaking C-C bonds:

Info autore

Vicente Gotor assumed his current position as Professor of Organic Chemistry at the University of Oviedo in 1982. His research fields include the areas of Heterocyclic and Bioorganic Chemistry. Specific areas of his research interest are enzymatic amidation reactions with hydrolases, enzymatic chemoselective transformations on natural products, biotransformations with oxynitrilases and oxidoreductases, and chiral recognition with azamacrocycles. He was Vice-chancellor of Research of Oviedo University for four years until June 2000. At present, he is the leader of Bioorganic group in the Chemistry Faculty of Oviedo University and Head of Department of Organic and Inorganic Chemistry. He has published more of 240 papers, is director of 40 Doctoral Thesis and coauthor of 10 patents.

Ignacio Alfonso completed his PhD in 1999 at the University of Oviedo, obtaining the PhD extraordinary award. During his doctoral studies, he spent a short period of time at the University of Strasbourg working under the supervision of Profs. Bernard Dietrich and Nobel Prize Winner Jean-Marie Lehn. After finishing his PhD, he moved to The Scripps Research Institute in La Jolla, California, as a postdoctoral fellow with Prof. M. Reza Ghadiri. Since 2004, he is researcher at the University Jaume I in Castellón, Spain. His research interests are bioorganic and supramolecular chemistry, biosensing, molecular recognition as well as natural and biomimetic catalytic systems.

Eduardo García-Urdiales graduated in Chemistry in 1996 at the University of Oviedo. He joined Prof. Gotor's group where he performed his PhD. After having finished it in 2001, he moved to Solvay Pharmaceuticals GmbH in Hannover (Germany) as a postdoctoral fellow in the Computer Aided Drug Design unit, where he stayed for two years (2001-2003). Then, he moved back to Oviedo and since 2005 he is working at the Russell Group at EMBL Heidelberg (Germany). His research interests are focussed on the study of protein-ligand interactions by means of computational methods.

Riassunto

Perfect for biochemists, synthetic and organic chemists, this book covers all important reactions, including C-C coupling reactions, oxidation reactions and many more.
Divided into two parts, the first section on methodology presents new innovative methods for enzymatic catalysis optimization, including such new trends as medium engineering, directed evolution and computer-aided prediction of enantioselectivity. The second and main section deals with applications to synthesis, showing important reaction types and their applications. Only those reactions with very high selectivity are presented, allowing readers to improve their own reaction yields.

Relazione

"An up-to-date insight into important enzyme-catalyzed reactions. The chapters comprise the most frequently used techniques and concepts with some very interesting new developments. The two complementary sections are useful, and the book can be recommended to a broad readership as an introductory guide for the use of enzymes in asymmetric organic synthesis." ( ChemSusChem , December 2008)
"...it provides a solid, up-to-date, and comprehensive introduction and overview of enzyme-catalyzed asymmetric synthesis, and can undoubtedly be recommended to students and lecturers..." ( Angewandte Chemie , August 18, 2008)

"Because the text covers a wide span of topics and resesarch interest, it is recommended as a learning tool fo rgraudate students in biochemistry and organic chemistry entering the field and as a guide to professionals aready enjoying the power of enzymes..." ( Journal of the American Chemical Society , August 13, 2008)

Dettagli sul prodotto

Autori Ignacio Alfonso, Eduardo García-Urdiales, Vicente Gotor
Con la collaborazione di Ignaci Alfonso (Editore), Ignacio Alfonso (Editore), Eduardo García-Urdiales (Editore), Vicente Gotor (Editore)
Editore Wiley-VCH
 
Lingue Inglese
Formato Copertina rigida
Pubblicazione 01.01.2008
 
EAN 9783527318254
ISBN 978-3-527-31825-4
Pagine 326
Dimensioni 180 mm x 242 mm x 21 mm
Peso 764 g
Illustrazioni 244 SW-Abb., 9 Farbabb., 13 Tabellen
Categorie Scienze naturali, medicina, informatica, tecnica > Chimica > Chimica organica

Chemie, Biochemie, Organische Chemie, Life Sciences, Biowissenschaften, biotechnology, chemistry, Organische Synthese, Biotechnologie i. d. Biowissenschaften, Enzyme u. Rezeptoren, Enzymes & Receptors, Methods - Synthesis & Techniques, Organische Chemie / Methoden, Synthesen, Verfahren, Biotechnologie i. d. Chemie, Asymmetrische Synthese

Recensioni dei clienti

Per questo articolo non c'è ancora nessuna recensione. Scrivi la prima recensione e aiuta gli altri utenti a scegliere.

Scrivi una recensione

Top o flop? Scrivi la tua recensione.

Per i messaggi a CeDe.ch si prega di utilizzare il modulo di contatto.

I campi contrassegnati da * sono obbligatori.

Inviando questo modulo si accetta la nostra dichiarazione protezione dati.