organic catalysis and material science. Other fields where a significant amount of new results has been obtained include nanotechnology,
self assembly/supramolecular systems and biochemical/medicinal chemistry. As a result, gold is one of the hottest topics in catalysis at
the moment, with an increasing amount of research being carried out in this field.
While focusing on homogeneous catalysis, this monograph also covers the main applications in heterogeneous catalysis. Following
a look at the gold-catalyzed addition of heteroatom nucleophiles to alkynes, it goes on to discuss gold-catalyzed additions to allenes and
alkenes, gold-catalyzed benzannulations, cycloisomerization and rearrangement reactions, as well as oxidation and reduction reactions.
The whole is finished off with a section on gold-catalyzed aldol and related reactions and the application of gold-catalyzed reactions to natural
product synthesis.
Of interest to synthetic chemists and inorganic chemists, as well as organic chemists working in homogeneous catalysis, physical and
technical chemists.
Stephen Hashmi is professor for Organic Chemistry at University of Heidelberg, Germany. He obtained his academic degrees from Ludwig-Maximilians-Universität München, after his postdoctoral studies with Barry M. Trost at Stanford University he started his Habilitation at Freie Universität Berlin with Johann Mulzer. During that time he followed Prof. Mulzer to Johann Wolfgang Goethe-Universität Franfurt and Universität Wien. He then returned to Frankfurt to finish his Habilitation. After the stations at University of Tasmania, Australia, Universität Marburg, and Universität Stuttgart, he was appointed a full professorship at Heidelberg University, where he is also involved in the Catalysis Research Laboratory (CaRLa). He received a number of awards, including a Karl-Zieger fellowship, the ORCHEM prize for natural scientists and the Hector research award. F. Dean Toste was born in Terceira, Azores, Portugal but soon moved to Toronto Canada. He received his B.Sc. and M.Sc. degrees in chemistry from the University of Toronto, Canada where he worked with Prof. Ian W. J. Still. In 1995, he began his doctoral studies at Stanford University under the direction of Professor Barry M. Trost. Following postdoctoral studies with Professor Robert H. Grubbs at Caltech, he joined the faculty at the University of California, Berkeley in 2002, and was promoted to Associate Professor in 2006 and Professor in 2009. Professor Toste?s honors include an Alfred P. Sloan Research Fellowship, the Cope Scholar Award and the E. J. Corey Award from the American Chemical Society, BASF Catalysis Award, the OMCOS and Thieme Award from IUPAC, the Merck Award from the Royal Society of Chemistry, the Mukaiyama Award, the Tetrahedron Young Investigator Award and numerous awards from the pharmaceutical industry.
HYDROCHLORINATION OF ACETYLENE CATALYZED BY GOLD
Introduction
Reactions of Alkynes Using Gold Chloride as Catalyst
The Correlation of E88 with the Activity of Gold for the Hydrochlorination of Acetylene
Central Role of Au3 p and Regeneration of Au/C Catalysts
Reaction Mechanism of Alkynes Over Au/C Catalysts
Chemical Origin of the E8 Correlation and General Remarks
Commercial Processes and Economic Aspects of Vinyl Chloride Monomer Manufacture
GOLD-CATALYZED REDUCTION REACTIONS
Introduction
Hydrogenation of Multiple C¼C Bonds. Role of the Gold Oxidation State
Hydrogenation of a,b-Unsaturated Aldehydes
Hydrogenation of Substituted Nitroaromatic Compounds
GOLD-CATALYZED BENZANNULATIONS: ASAO - YAMAMOTO BENZOPYRYLIUM PATHWAY
Introduction
Acetylenic Compounds as 2p Systems
Enols as 2p Systems
Enol Ethers as 2p Systems
Benzynes as 2p Systems
Synthesis of Phthalazine Derivatives
Application to the Synthesis of Angucyclinone Antibiotics and Other Applications in Total Synthesis
Copper-Catalyzed Benzannulations
Conclusion
GOLD-CATALYZED REACTIONS OF PROPARGYL ESTERS, PROPARGYL ALCOHOLS, AND RELATED COMPOUNDS
Introduction and Extent of This Chapter
Propargyl Esters
Propargyl Ethers
Propargyl Alcohols
Propargyl Amines
Propargyl Carbonates, Amides, and Carbamates
Other Propargyl Substitution Patterns
Conclusion
INTRAMOLECULAR HYDROARYLATION OF ALKYNES
Introduction
Intramolecular Reactions of Arenes with Alkynes
Intramolecular Reactions of Electron-Rich Heteroarenes with Alkynes
Conclusion and Outlook
GOLD - ALKYNE COMPLEXES
Introduction
Description of the M - p-Bond Interaction in Alkene and Alkyne Complexes
Gold(0) Complexes
Gold(I) Complexes
Gold(III) complexes
Theoretical Studies
GOLD - ALKENE COMPLEXES
Introduction
Gold(0) Derivatives
Gold(I) Complexes
Gold(III) Complexes
Theoretical Studies
HYDRATION AND HYDROALKOXYLATION OF CC MULTIPLE BONDS
Historical Perspective
Gold Catalysts
Hydration and Hydroalkoxylation of CC Triple Bonds (Alkynes)
Hydration and Hydroalkoxylation of CC Double Bonds (Allenes and Alkenes)
GOLD-CATALYZED ALDOL AND RELATED REACTIONS
The Gold-Catalyzed Aldol Reaction
Related Reactions
GOLD-CATALYZED OXIDATION REACTIONS: OXIDATION OF ALKENES
Introduction
Epoxidation Reactions
Aziridination Reactions
Oxidative Cleavage of C¼C Double Bonds
Oxygen Transfer to Carbenoids
GOLD-CATALYZED OXYGEN-ATOM TRANSFER TO ALKYNES
Introduction
Oxygen-Atom Transfer from NO Groups
Oxygen-Atom Transfer from Sulfoxides
Oxygen-Atom Transfer from Epoxides
Gold-Catalyzed Oxidative Coupling
GOLD-CATALYZED ADDITIONS TO ALKENES: N-NUCLEOPHILES
GOLD-CATALYZED ADDITIONS TO ALKENES: O-NUCLEOPHILES
OXIDATION OF ALCOHOLS AND CARBOHYDRATES
Introduction
Selective Oxidation of Alcohols
Selective Oxidation of Carbohydrates
Future Applications
Conclusion
APPLICATIONS OF GOLD-CATALYZED REACTIONS TO NATURAL PRODUCT SYNTHESIS
Introduction
Addition of Heteroatom Nucleophiles to Alkynes
Addition of Heteroatom Nucleophiles to Allenes
Cycloadditions via Pyrylium Intermediates from o-Alkynylacylarenes
Rearrangements of Propargyl Esters
Skeletal Rearrangement of 3-Butynyl-N-Oxides: (_)-Cermizine and (?)-Lentiginosine
Enyne Cyclizations
Propargyl Claisen Rearrangement: Azadirachtin
Gold-Catalyzed C?H Activation: (_)-Pterocarpan and Crassifolone
Gold-Catalyzed Allylic Amination: (_)-Angustureine
Catalytic Asymmetric Aldol Reaction of Isocyanoacetates and Aldehydes
GOLD-CATALYZED ADDITION REACTIONS TO ALLENES
Introduction
Addition of Heteroatom Nucleophiles
Addition of Carbon Nucleophiles
Conclusion
Erscheint lt. Verlag | 6.4.2012 |
---|---|
Sprache | englisch |
Themenwelt | Naturwissenschaften ► Chemie ► Organische Chemie |
Technik | |
Schlagworte | catalysis • Chemie • Chemische Synthese • Chemistry • Coordination Chemistry • gold nanoparticle catalysis, luminiscent organogold compounds, molecular self assembly, supramolecular systems, gold heterogeneous catalysis, gold homogeneous catalysis, organic chemistry, materials science, organometallics • Katalyse • Koordinationschemie • Methods - Synthesis & Techniques • Organic Chemistry • Organische Chemie • Organische Chemie / Methoden, Synthesen, Verfahren • Organische Synthese |
ISBN-10 | 3-527-64688-4 / 3527646884 |
ISBN-13 | 978-3-527-64688-3 / 9783527646883 |
Haben Sie eine Frage zum Produkt? |
Größe: 5,8 MB
Kopierschutz: Adobe-DRM
Adobe-DRM ist ein Kopierschutz, der das eBook vor Mißbrauch schützen soll. Dabei wird das eBook bereits beim Download auf Ihre persönliche Adobe-ID autorisiert. Lesen können Sie das eBook dann nur auf den Geräten, welche ebenfalls auf Ihre Adobe-ID registriert sind.
Details zum Adobe-DRM
Dateiformat: EPUB (Electronic Publication)
EPUB ist ein offener Standard für eBooks und eignet sich besonders zur Darstellung von Belletristik und Sachbüchern. Der Fließtext wird dynamisch an die Display- und Schriftgröße angepasst. Auch für mobile Lesegeräte ist EPUB daher gut geeignet.
Systemvoraussetzungen:
PC/Mac: Mit einem PC oder Mac können Sie dieses eBook lesen. Sie benötigen eine
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 eine
Geräteliste und zusätzliche Hinweise
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.
aus dem Bereich