Modern Gold Catalyzed Synthesis
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More About This Title Modern Gold Catalyzed Synthesis
English
With its impressive features, gold has led to completely new reaction types in recent years, which in turn have strongly influenced both
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.
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.
English
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.
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.
English
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
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
English
“In conclusion, this well-written book is recommended to both synthetic chemists and those involved in the study of catalysis.” (Organic Process Research & Development, 1 May 2013)
