Visible Light Photocatalyzed Redox-Neutral Organic Reactions and Synthesis of Novel Metal-Organic Frameworks. (2016)
- Record Type:
- Book
- Title:
- Visible Light Photocatalyzed Redox-Neutral Organic Reactions and Synthesis of Novel Metal-Organic Frameworks. (2016)
- Main Title:
- Visible Light Photocatalyzed Redox-Neutral Organic Reactions and Synthesis of Novel Metal-Organic Frameworks.
- Other Names:
- Sahoo, Basudev
- Contents:
- Supervisor's Foreword; Abstract; Parts of this thesis have been published in the following journal articles:; Acknowledgements; Contents; Abbreviations; 1 Introduction to Photocatalysis; 1.1 Historical Background; 1.2 Classifications of Photocatalyst; 1.3 Characteristics of Homogeneous Photocatalysts; 1.4 Visible Light Photocatalysis in Organic Synthesis; 1.4.1 Photoredox Catalyzed Organic Transformations via Electron Transfer; 1.4.1.1 Redox-Neutral Photoredox Catalysis: Single Catalysis; 1.4.1.2 Photoredox Catalysis: Dual Catalysis (Transition Metal). 1.4.1.3 Redox-Neutral Photoredox Catalysis: EDA Complex Formation1.4.2 Photocatalyzed Organic Transformations via Triplet Energy Transfer; 1.5 Summary; References; 2 Dual Gold and Visible Light Photoredox-Catalyzed Heteroarylations of Non-activated Alkenes; 2.1 Introduction; 2.1.1 General Properties of Homogeneous Gold Catalysts; 2.1.2 Gold-Catalyzed Organic Transformations; 2.1.2.1 Historical Background; 2.1.2.2 Difunctionalizations of Carbon-Carbon Multiple Bonds: Mechanistic Hypothesis; Organogold Reactivity in Dual Metal Catalysis; Nucleophilic Addition/Rearrangement-Oxidative Coupling. 2.1.3 Aryldiazonium Salts: Synthesis and Reactivity2.1.4 Diaryliodonium Salts: Synthesis and Reactivity; 2.2 Results and Discussion; 2.2.1 Inspiration; 2.2.2 Intramolecular Oxy- and Aminoarylation of Alkenes; 2.2.2.1 Preliminary Tests and Optimization Studies; 2.2.2.2 Substrate Scope and Limitations; 2.2.3 Intermolecular Oxyarylation ofSupervisor's Foreword; Abstract; Parts of this thesis have been published in the following journal articles:; Acknowledgements; Contents; Abbreviations; 1 Introduction to Photocatalysis; 1.1 Historical Background; 1.2 Classifications of Photocatalyst; 1.3 Characteristics of Homogeneous Photocatalysts; 1.4 Visible Light Photocatalysis in Organic Synthesis; 1.4.1 Photoredox Catalyzed Organic Transformations via Electron Transfer; 1.4.1.1 Redox-Neutral Photoredox Catalysis: Single Catalysis; 1.4.1.2 Photoredox Catalysis: Dual Catalysis (Transition Metal). 1.4.1.3 Redox-Neutral Photoredox Catalysis: EDA Complex Formation1.4.2 Photocatalyzed Organic Transformations via Triplet Energy Transfer; 1.5 Summary; References; 2 Dual Gold and Visible Light Photoredox-Catalyzed Heteroarylations of Non-activated Alkenes; 2.1 Introduction; 2.1.1 General Properties of Homogeneous Gold Catalysts; 2.1.2 Gold-Catalyzed Organic Transformations; 2.1.2.1 Historical Background; 2.1.2.2 Difunctionalizations of Carbon-Carbon Multiple Bonds: Mechanistic Hypothesis; Organogold Reactivity in Dual Metal Catalysis; Nucleophilic Addition/Rearrangement-Oxidative Coupling. 2.1.3 Aryldiazonium Salts: Synthesis and Reactivity2.1.4 Diaryliodonium Salts: Synthesis and Reactivity; 2.2 Results and Discussion; 2.2.1 Inspiration; 2.2.2 Intramolecular Oxy- and Aminoarylation of Alkenes; 2.2.2.1 Preliminary Tests and Optimization Studies; 2.2.2.2 Substrate Scope and Limitations; 2.2.3 Intermolecular Oxyarylation of Alkenes; 2.2.3.1 Preliminary Tests and Optimization Studies; 2.2.3.2 Substrate Scope and Limitations; 2.2.4 Mechanistic Studies on Heteroarylations of Alkenes; 2.3 Summary; References. 3 Visible Light Photoredox Catalyzed Trifluoromethylation-Ring Expansion via Semipinacol Rearrangement3.1 Introduction; 3.1.1 General Features of Fluorinated Compounds; 3.1.2 Importances of Fluorinated Compounds; 3.1.3 Radical-Polar Crossover Process; 3.1.4 Trifluoromethylation of Alkenes; 3.1.4.1 Trifluoromethylating Reagents; 3.1.4.2 Classifications of Trifluoromethylated Compounds and Trifluoromethylation; 3.1.4.3 Visible Light Photoredox-Catalyzed Trifluoromethylations via Radical-Polar Crossover; 3.1.5 Semipinacol Rearrangements; 3.2 Results and Discussion; 3.2.1 Inspiration. 3.2.2 Preliminary Experiments and Optimization Studies3.2.3 Substrate Scope and Limitations; 3.2.4 Follow up Transformations of Products; 3.2.5 Mechanistic Studies; 3.3 Summary; References; 4 Transition Metal Free Visible Light-Mediated Synthesis of Polycyclic Indolizines; 4.1 Introduction; 4.1.1 General Properties of Indolizines; 4.1.2 Importances of Indolizines; 4.1.3 Synthesis of Indolizines; 4.1.3.1 Synthesis of Indolizines via Methine Formation; 4.1.3.2 Synthesis of Indolizines via a 1, 3-Dipolar Cycloaddition; 4.1.3.3 Synthesis of Indolizines via a 1, 5-Dipolar Cyclization. … (more)
- Publisher Details:
- Cham, SWITZERLAND : Springer
- Publication Date:
- 2016
- Extent:
- 1 online resource (274)
- Subjects:
- 540
Chemistry
Photocatalysis
SCIENCE -- Chemistry -- Physical & Theoretical
Photocatalysis
Science -- Chemistry -- Industrial & Technical
Catalysis
Industrial chemistry
Chemistry, Organic
Catalysis
Chemical engineering
Science -- Chemistry -- Organic
Organic chemistry
Electronic books - Languages:
- English
- ISBNs:
- 3319483501
9783319483504 - Related ISBNs:
- 3319483498
9783319483498 - Notes:
- Note: Includes bibliographical references.
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