Au-catalyzed synthesis and functionalization of heterocycles. (2016)
- Record Type:
- Book
- Title:
- Au-catalyzed synthesis and functionalization of heterocycles. (2016)
- Main Title:
- Au-catalyzed synthesis and functionalization of heterocycles
- Further Information:
- Note: Marco Bandini, editor ; with contributions by N. Ahlsten [and more].
- Editors:
- Bandini, Marco
- Contents:
- Intro; Preface; Contents; Synthesis of Oxygenated Heterocyclic Compounds via Gold-Catalyzed Functionalization of pi-Systems; 1 Introduction; 2 Oxycyclizations Initiated by a Gold-Promoted Activation of pi-Bonds; 2.1 Cycloisomerizations Involving Hydroalkoxylations and Hydrocarboxylations of pi-Systems; 2.1.1 Hydroalkoxylation of Allenes; 2.1.2 Hydrocarboxylation of Allenes; 2.1.3 Hydroalkoxylation of Alkynes; 2.1.4 Hydrocarboxylation of Alkynes; 2.1.5 Hydroalkoxylation of Alkenes; 2.2 Cycloisomerizations of Allenyl and Alkynyl Ketones, and Alkynyl Epoxides; 2.3 Cycloisomerization Cascades 2.3.1 Cycloisomerization Cascades Initiated by Activation of Alkynes2.3.2 Cycloisomerization Cascades Initiated by Activation of Allenes; 2.3.3 Cycloisomerization Cascades Involving a Gold-Promoted Activation of Alkenes; 2.4 Oxycyclizations with the Participation of Additional Exogenous Components; 2.4.1 Incorporation of Oxygen-Based Nucleophiles (H2O, ROH); 2.4.2 Participation of Other Type of Exogenous Components; 3 Cycloisomerizations Involving Rearrangements; 3.1 Oxycyclizations Preceded by Rearrangements of Propargylic Esters; 3.2 Oxycyclizations Preceded by Enyne Cycloisomerizations 3.3 Oxycyclizations Followed by Rearrangements3.4 1, 5-Hydrogen Migrations; 4 Formal Cycloadditions; 4.1 Cycloadditions Based on the Gold-Promoted Generation of Reactive Dipoles; 4.2 Other Formal Gold-Catalyzed Cycloadditions Involving Stepwise Processes; 5 Conclusions; References; Gold-Catalyzed SynthesisIntro; Preface; Contents; Synthesis of Oxygenated Heterocyclic Compounds via Gold-Catalyzed Functionalization of pi-Systems; 1 Introduction; 2 Oxycyclizations Initiated by a Gold-Promoted Activation of pi-Bonds; 2.1 Cycloisomerizations Involving Hydroalkoxylations and Hydrocarboxylations of pi-Systems; 2.1.1 Hydroalkoxylation of Allenes; 2.1.2 Hydrocarboxylation of Allenes; 2.1.3 Hydroalkoxylation of Alkynes; 2.1.4 Hydrocarboxylation of Alkynes; 2.1.5 Hydroalkoxylation of Alkenes; 2.2 Cycloisomerizations of Allenyl and Alkynyl Ketones, and Alkynyl Epoxides; 2.3 Cycloisomerization Cascades 2.3.1 Cycloisomerization Cascades Initiated by Activation of Alkynes2.3.2 Cycloisomerization Cascades Initiated by Activation of Allenes; 2.3.3 Cycloisomerization Cascades Involving a Gold-Promoted Activation of Alkenes; 2.4 Oxycyclizations with the Participation of Additional Exogenous Components; 2.4.1 Incorporation of Oxygen-Based Nucleophiles (H2O, ROH); 2.4.2 Participation of Other Type of Exogenous Components; 3 Cycloisomerizations Involving Rearrangements; 3.1 Oxycyclizations Preceded by Rearrangements of Propargylic Esters; 3.2 Oxycyclizations Preceded by Enyne Cycloisomerizations 3.3 Oxycyclizations Followed by Rearrangements3.4 1, 5-Hydrogen Migrations; 4 Formal Cycloadditions; 4.1 Cycloadditions Based on the Gold-Promoted Generation of Reactive Dipoles; 4.2 Other Formal Gold-Catalyzed Cycloadditions Involving Stepwise Processes; 5 Conclusions; References; Gold-Catalyzed Synthesis of Nitrogen Heterocyclic Compounds via Hydroamination Reactions; 1 Introduction; 2 Synthesis of Nitrogen Heterocyclic Compounds Through Gold-Catalyzed Intramolecular Hydroamination of Alkynes; 3 Gold-Catalyzed Annulation Reactions of Aminoallenes 4 Gold-Catalyzed Intramolecular Hydroamination of Unconjugated Alkenes5 Synthesis of Nitrogen Heterocyclic Compounds Through Sequential Gold-Catalyzed Processes Implying a Hydroamination Step; 6 Conclusion; References; Synthesis of Oxygenated and Nitrogen-Containing Heterocycles by Gold-Catalyzed Alkyne Oxidation; 1 Introduction; 2 Synthesis of Oxygenated Heterocycles; 2.1 Reaction with Terminal Alkynes; 2.2 Reaction with Internal Alkynes; 3 Synthesis of Nitrogen-Containing Heterocycles; 3.1 Reactions of Alkyne Substrates with Tethered Oxidants 3.1.1 O-Nitro or O-Nitrone as Oxidants in the Reactions of Arylalkynes3.1.2 Pyridine N-Oxides as Oxidants; 3.1.3 Tertiary Amine N-Oxides as Oxidants; 3.2 Reactions of Alkyne Substrates with External Oxidants; 3.2.1 Reaction with Tethered Nucleophiles; 3.2.2 Reaction with External Nucleophiles; 3.2.3 Oxidants or Parts of Them Incorporated into Products; 4 Conclusions; References; Synthesis of Heterocyclic Compounds via Gold-Catalysed Enyne Rearrangements; 1 Introduction; 2 Gold-Enyne Coordination; 3 Gold-Catalysed Enyne Cycloisomerisation by Skeletal Rearrangement; 3.1 Mechanistic Insights … (more)
- Publisher Details:
- Switzerland : Springer
- Publication Date:
- 2016
- Extent:
- 1 online resource (vii, 289 pages), illustrations (some color)
- Subjects:
- 547/.59
Chemistry
Heterocyclic compounds -- Synthesis
Metal catalysts
Gold
Gold
Heterocyclic compounds -- Synthesis
Metal catalysts
Science -- Chemistry -- Organic
Science -- Chemistry -- Industrial & Technical
Carbohydrates
Catalysis
Chemistry, Organic
Carbohydrates
Catalysis
Organometallic chemistry
Electronic books - Languages:
- English
- ISBNs:
- 9783319351445
3319351443
3319351427
9783319351421 - Related ISBNs:
- 9783319351421
- Notes:
- Note: Includes bibliographical references and index.
Note: Online resource; title from PDF title page (SpringerLink, viewed July 11, 2016). - Access Rights:
- Legal Deposit; Only available on premises controlled by the deposit library and to one user at any one time; The Legal Deposit Libraries (Non-Print Works) Regulations (UK).
- Access Usage:
- Restricted: Printing from this resource is governed by The Legal Deposit Libraries (Non-Print Works) Regulations (UK) and UK copyright law currently in force.
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD.DS.370018
- Ingest File:
- 01_354.xml