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120430s2012 xx o 000 0 eng d |
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|a 500
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|a UAMI
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|a Hashmi, A. Stephen K.
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|a Modern Gold Catalyzed Synthesis.
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|a Hoboken :
|b John Wiley & Sons,
|c 2012.
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|a 1 online resource (604 pages)
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
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|a Cover; Further Reading; Title Page; Copyright; List of Contributers; Chapter 1: Hydrochlorination of Acetylene Catalyzed by Gold; 1.1 Introduction; 1.2 Reactions of Alkynes Using Gold Chloride as Catalyst; 1.3 The Correlation of E° with the Activity of Gold for the Hydrochlorination of Acetylene; 1.4 Central Role of Au3+ and Regeneration of Au/C Catalysts; 1.5 Reaction Mechanism of Alkynes Over Au/C Catalysts; 1.6 Chemical Origin of the E° Correlation and General Remarks; 1.7 Commercial Processes and Economic Aspects of Vinyl Chloride Monomer Manufacture; References.
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|a Chapter 2: Gold-Catalyzed Reduction Reactions2.1 Introduction; 2.2 Hydrogenation of Multiple C=C Bonds. Role of the Gold Oxidation State; 2.3 Hydrogenation of a, ß-Unsaturated Aldehydes; 2.4 Hydrogenation of Substituted Nitroaromatic Compounds; References; Chapter 3: Gold-Catalyzed Benzannulations: Asao-Yamamoto Benzopyrylium Pathway; 3.1 Introduction; 3.2 Acetylenic Compounds as 2p Systems; 3.3 Enols as 2p Systems; 3.4 Enol Ethers as 2p Systems; 3.5 Benzynes as 2p Systems; 3.6 Synthesis of Phthalazine Derivatives.
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|a 3.7 Application to the Synthesis of Angucyclinone Antibiotics and Other Applications in Total Synthesis3.8 Copper-Catalyzed Benzannulations; 3.9 Conclusion; References; Chapter 4: Gold-Catalyzed Reactions of Propargyl Esters, Propargyl Alcohols, and Related Compounds; 4.1 Introduction and Extent of This Chapter; 4.2 Propargyl Esters; 4.3 Propargyl Ethers; 4.4 Propargyl Alcohols; 4.5 Propargyl Amines; 4.6 Propargyl Carbonates, Amides, and Carbamates; 4.7 Other Propargyl Substitution Patterns; 4.8 Conclusion; Reagent Abbreviations; References; Chapter 5: Intramolecular Hydroarylation of Alkynes.
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|a 5.1 Introduction5.2 Intramolecular Reactions of Arenes with Alkynes; 5.3 Intramolecular Reactions of Electron-Rich Heteroarenes with Alkynes; 5.4 Conclusion and Outlook; Acknowledgments; References; Chapter 6: Gold-Alkyne Complexes; 6.1 Introduction; 6.2 Description of the M-p-Bond Interaction in Alkene and Alkyne Complexes; 6.3 Gold(0) Complexes; 6.4 Gold(I) Complexes; 6.5 Gold(III) complexes; 6.6 Theoretical Studies; References; Chapter 7: Gold-Alkene Complexes; 7.1 Introduction; 7.2 Gold(0) Derivatives; 7.3 Gold(I) Complexes; 7.4 Gold(III) Complexes; 7.5 Theoretical Studies; References.
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|a Chapter 8: Hydration and Hydroalkoxylation of CC Multiple Bonds8.1 Historical Perspective; 8.2 Gold Catalysts; 8.3 Hydration and Hydroalkoxylation of CC Triple Bonds (Alkynes); 8.4 Hydration and Hydroalkoxylation of CC Double Bonds (Allenes and Alkenes); References; Chapter 9: Gold-Catalyzed Aldol and Related Reactions; 9.1 The Gold-Catalyzed Aldol Reaction; 9.2 Related Reactions; Acknowledgement; References; Chapter 10: Gold-Catalyzed Oxidation Reactions: Oxidation of Alkenes; 10.1 Introduction; 10.2 Epoxidation Reactions; 10.3 Aziridination Reactions.
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|a 10.4 Oxidative Cleavage of C?C Double Bonds.
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|a With its impressive features, gold has added another facet to organic catalysis. Focusing on homogeneous catalysis this book also covers the main applications in heterogeneous catalysis. Following a look at the gold-catalyzed addition of heteroatom nucleophiles to alkynes, this monograph 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-cat.
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|a Print version record.
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|a ProQuest Ebook Central
|b Ebook Central Academic Complete
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|a Catalysis.
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|a Gold.
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|a Organic compounds
|x Synthesis.
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|a Transition metal catalysts.
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|a Catalysis
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|a Gold
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|a Catalysis.
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|a Ring formation (Chemistry)
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|a Catalyse.
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|a Or.
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|a Composés organiques
|x Synthèse.
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|a Catalyseurs à base de métaux de transition.
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|a teocuitlatl.
|2 aat
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|a gold (metal)
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|a Catalysis
|2 fast
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|a Gold
|2 fast
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|a Organic compounds
|x Synthesis
|2 fast
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|a Transition metal catalysts
|2 fast
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|a Toste, F. Dean.
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|i has work:
|a Modern gold catalyzed synthesis (Text)
|1 https://id.oclc.org/worldcat/entity/E39PCGWg9KcQbkp4bQDGyCFCXq
|4 https://id.oclc.org/worldcat/ontology/hasWork
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|i Print version:
|a Hashmi, A. Stephen K.
|t Modern Gold Catalyzed Synthesis.
|d Hoboken : John Wiley & Sons, ©2012
|z 9783527319527
|
856 |
4 |
0 |
|u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=896061
|z Texto completo
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938 |
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|a Askews and Holts Library Services
|b ASKH
|n AH23079892
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938 |
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|a EBL - Ebook Library
|b EBLB
|n EBL4044312
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938 |
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|a EBL - Ebook Library
|b EBLB
|n EBL896061
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|a ProQuest MyiLibrary Digital eBook Collection
|b IDEB
|n 364033
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|a 92
|b IZTAP
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