Asymmetric Organocatalysis in Natural Product Syntheses (eBook)

(Autor)

eBook Download: PDF
2012 | 2012
XI, 197 Seiten
Springer Wien (Verlag)
978-3-7091-1163-5 (ISBN)

Lese- und Medienproben

Asymmetric Organocatalysis in Natural Product Syntheses - Mario Waser
Systemvoraussetzungen
213,99 inkl. MwSt
  • Download sofort lieferbar
  • Zahlungsarten anzeigen
This book provides the reader with an illustrative overview concerning successful and widely used applications of organocatalysis in the field of natural product synthesis. The main focus will be on organocatalytic key-steps for each (multi-step) synthesis described, whereas other often particularly innovative transformations will be omitted, as this would be beyond the scope of this volume.

Mario Waser was born in Steyr, Austria in 1977. After studying chemistry at the Johannes Kepler University (JKU) Linz, Austria, he finished his Ph.D. thesis in 2005 in the group of Prof. Dr. Heinz Falk, working on the synthesis of second-generation hypericin-based photosensitizers. After a postdoctoral stay in the group of Prof. Dr. Alois Fürstner at the Max-Planck Institut für Kohlenforschung (Mülheim, Germany), investigating the first total syntheses of iejimalide B and iejimalide A, he spent two years as a research and development chemist for DSM Linz. Since the summer of 2009 he has held the position of Assistant Professor at JKU Linz, where he is currently working on his habilitation. Dr. Waser's main research interests are focused in the field of synthetic organic chemistry with a special emphasis on ammonium ylide-mediated (dia)-stereoselective reactions and the design of new tartaric acid-derived organocatalysts.

Mario Waser was born in Steyr, Austria in 1977. After studying chemistry at the Johannes Kepler University (JKU) Linz, Austria, he finished his Ph.D. thesis in 2005 in the group of Prof. Dr. Heinz Falk, working on the synthesis of second-generation hypericin-based photosensitizers. After a postdoctoral stay in the group of Prof. Dr. Alois Fürstner at the Max-Planck Institut für Kohlenforschung (Mülheim, Germany), investigating the first total syntheses of iejimalide B and iejimalide A, he spent two years as a research and development chemist for DSM Linz. Since the summer of 2009 he has held the position of Assistant Professor at JKU Linz, where he is currently working on his habilitation. Dr. Waser’s main research interests are focused in the field of synthetic organic chemistry with a special emphasis on ammonium ylide-mediated (dia)-stereoselective reactions and the design of new tartaric acid-derived organocatalysts.

1 Introduction.- 2 Enamine Catalysis.- Aldol Reactions.- Mannich Reactions.- a-Heterofunctionalizations.- Conjugate Additions.- Dienamine Catalysis.- Combined Enamine-Catalyzed Approaches and Cascade Reactions.- Synopsis.- 3 Iminium Catalysis.- Pericyclic Reactions.- Conjugate Additions.- Iminium-Catalyzed Organocascade Reactions.- Synopsis.- 4 Combined Iminium-Enamine Catalyzed Approaches.- Cascade Reactions Using a Single Organocatalyst.- Organocascade Catalysis Using a Combination of Different Catalysts.- Synopsis.- 5 Singly Occupied Molecular Orbital (SOMO) Catalysis.- Friedel-Crafts Reactions.- Epoxide Formation.- Synopsis.- 6 Asymmetric Phase-Transfer Catalysis.- Asymmetric a-Alkylations.- Phase-Transfer Catalyzed Michael Additions.- Alkylative Dearomatization-Annulation Reaction.- Synopsis.- 7 Chiral Brønsted Acids and Hydrogen Bonding Donors.- Chiral Phosphoric Acids.- Chiral Diols.- Chiral (Thio)-Ureas.- Bifunctional Brønsted Acid-Base Active (Thio)-Ureas.- Synopsis.- 8 Chiral Brønsted and Lewis Bases.- Cinchona Alkaloids.- Phosphine Catalysis.- Carbene Catalysis.- Synopsis.- 9 Asymmetric Oxidations and Reductions.- Organocatalytic Oxidations.- Organocatalytic Reductions.- Synopsis.- 10 Conclusions.

Erscheint lt. Verlag 30.7.2012
Reihe/Serie Progress in the Chemistry of Organic Natural Products
Progress in the Chemistry of Organic Natural Products
Zusatzinfo XI, 197 p.
Verlagsort Vienna
Sprache englisch
Themenwelt Naturwissenschaften Chemie Organische Chemie
Technik
Schlagworte Chiral Brønsted Acids • Enamine Catalysis • Iminium Catalysis • Single Occupied Molecular Orbital (SOMO) catalysis
ISBN-10 3-7091-1163-3 / 3709111633
ISBN-13 978-3-7091-1163-5 / 9783709111635
Haben Sie eine Frage zum Produkt?
PDFPDF (Wasserzeichen)
Größe: 8,0 MB

DRM: Digitales Wasserzeichen
Dieses eBook enthält ein digitales Wasser­zeichen und ist damit für Sie persona­lisiert. Bei einer missbräuch­lichen Weiter­gabe des eBooks an Dritte ist eine Rück­ver­folgung an die Quelle möglich.

Dateiformat: PDF (Portable Document Format)
Mit einem festen Seiten­layout eignet sich die PDF besonders für Fach­bücher mit Spalten, Tabellen und Abbild­ungen. Eine PDF kann auf fast allen Geräten ange­zeigt werden, ist aber für kleine Displays (Smart­phone, eReader) nur einge­schränkt geeignet.

Systemvoraussetzungen:
PC/Mac: Mit einem PC oder Mac können Sie dieses eBook lesen. Sie benötigen dafür einen PDF-Viewer - z.B. den Adobe Reader oder Adobe Digital Editions.
eReader: Dieses eBook kann mit (fast) allen eBook-Readern gelesen werden. Mit dem amazon-Kindle ist es aber nicht kompatibel.
Smartphone/Tablet: Egal ob Apple oder Android, dieses eBook können Sie lesen. Sie benötigen dafür einen PDF-Viewer - z.B. die kostenlose Adobe Digital Editions-App.

Zusätzliches Feature: Online Lesen
Dieses eBook können Sie zusätzlich zum Download auch online im Webbrowser lesen.

Buying eBooks from abroad
For tax law reasons we can sell eBooks just within Germany and Switzerland. Regrettably we cannot fulfill eBook-orders from other countries.

Mehr entdecken
aus dem Bereich
Das Basiswissen der Chemie

von Charles E. Mortimer; Ulrich Müller

eBook Download (2019)
Georg Thieme Verlag KG
84,99