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Sustainable catalysis, Without metals or other endangered elements. Part 2 /
Catalysis is a fundamentally sustainable process which can be used to produce a wide range of chemicals and their intermediates. Focussing on those catalytic processes which offer the most sustainability, this two-part book explores recent developments in this field, as well as examining future chal...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
[Cambridge] :
Royal Society of Chemistry,
[2015]
|
| Colección: | RSC green chemistry series ;
41. |
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 245 | 0 | 0 | |a Sustainable catalysis, |p Without metals or other endangered elements. |n Part 2 / |c editor: Michael North. |
| 246 | 3 | 0 | |a Without metals or other endangered elements. |n Part 2 |
| 264 | 1 | |a [Cambridge] : |b Royal Society of Chemistry, |c [2015] | |
| 264 | 4 | |c ©2016 | |
| 300 | |a 1 online resource | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 1 | |a RSC green chemistry ; |v 41 | |
| 520 | |a Catalysis is a fundamentally sustainable process which can be used to produce a wide range of chemicals and their intermediates. Focussing on those catalytic processes which offer the most sustainability, this two-part book explores recent developments in this field, as well as examining future challenges. Focussing on catalysis without metals or other endangered elements, each chapter covers a different type of organocatalyst. Beginning with chapters on acid and base catalysis, the book then concentrates on asymmetric catalysis. Several chapters cover pyrrolidine-based and cinchona alkaloid-based catalysts, whilst other chapters examine further organoctalysts which are constructed only from sustainable elements. Together with Sustainable Catalysis: With Non-endangered Metals, these books examine the progress in sustainable catalysis in all areas of chemistry, and are an important reference for researchers working in catalysis and green chemistry. | ||
| 500 | |a Includes index. | ||
| 588 | 0 | |a Online resource; title from title details screen (Royal Society of Chemistry, viewed November 19, 2015). | |
| 588 | 0 | |a Print version record. | |
| 504 | |a Includes bibliographical references at the end of each chapters and index. | ||
| 546 | |a English. | ||
| 505 | 8 | |a 16.2.1 Monoalkylation of Schiff Bases Derived from Glycine16.2.2 Dialkylation of Schiff Bases Derived from Glycine; 16.2.3 Other Alkylations with Cinchona-derived PTC Catalysts; 16.2.4 Conjugate Additions with Cinchona-derived PTC Catalysts; 16.2.5 Aldol Reactions with Cinchona-derived PTC Catalysts; 16.2.6 Mannich Reactions with Cinchona-derived PTC Catalysts; 16.2.7 Darzens Reaction with Cinchona-derived PTC Catalysts; 16.2.8 Epoxidation of Enones with Cinchona-derived PTC Catalysts; 16.2.9 Other Reactions with Cinchona-derived PTC Catalysts; 16.3 Conclusions; References. | |
| 505 | 8 | |a Chapter 17 Binaphthyl-derived Cyclic Amines and Their Salts as Asymmetric Organocatalysts 17.1 Introduction; 17.2 Design of Chiral Amine Catalysts; 17.2.1 Aldol Reactions; 17.2.2 Mannich Reactions; 17.2.3 Conjugate Additions; 17.2.4 C-O and C-N Bond Formations; 17.2.5 Halogenations; 17.3 Design of Chiral Phase-transfer Catalysts; 17.3.1 Alkylations; 17.3.2 Conjugate Additions; 17.3.3 Aldol and Mannich Reactions; 17.3.4 Strecker Reactions; 17.3.5 Oxidations; 17.4 Conclusions; References; Chapter 18 Imidazolidinones as Asymmetric Organocatalysts ; 18.1 Introduction. | |
| 505 | 0 | |a Cover; Contents; Preface; References; Part 2; Chapter 14 Nonquaternised Cinchona Alkaloid Derivatives as Asymmetric Organocatalysts for Carbon-Carbon Bond-forming Reactions ; 14.1 Introduction; 14.2 Catalytic Asymmetric 1,4-Addition Reactions; 14.3 Catalytic Asymmetric 1,2-Addition Reactions; 14.4 Catalytic Asymmetric Cycloaddition Reactions; 14.5 Concluding Remarks; References; Chapter 15 Nonquaternised Cinchona Alkaloid Derivatives as Asymmetric Organocatalysts for Carbon-Heteroatom Bond-forming Reactions ; 15.1 Introduction; 15.2 Hydrophosphonylation; 15.3 Epoxidation and Hydroperoxidation. | |
| 505 | 8 | |a 15.4 Aziridination15.5 Lactone and Lactam Formation; 15.6 Epoxide and Aziridine Ring Opening; 15.7 Anhydride Ring Opening; 15.8 Amination; 15.8.1 Amination by Substitution; 15.8.2 Aza-Michael Addition; 15.9 Hydroxylation; 15.9.1 Carbonyl (Sa (B-Hydroxylation ; 15.9.2 Oxa-Michael Addition; 15.10 Sulfenylation; 15.10.1 (Sa (B-Sulfenylation ; 15.10.2 Sulfa-Michael Addition; 15.11 Halogenation; References; Chapter 16 Cinchona Alkaloid Derivatives as Asymmetric Phase-transfer Catalysts ; 16.1 N-Quaternised Cinchona Alkaloid Ammonium Salts; 16.2 Asymmetric Phase-transfer Catalysis (PTC). | |
| 590 | |a Knovel |b ACADEMIC - Chemistry & Chemical Engineering | ||
| 650 | 0 | |a Catalysis. | |
| 650 | 2 | |a Catalysis | |
| 650 | 6 | |a Catalyse. | |
| 650 | 7 | |a Sustainability. |2 bicssc | |
| 650 | 7 | |a SCIENCE |x Chemistry |x Physical & Theoretical. |2 bisacsh | |
| 650 | 7 | |a Catalysis |2 fast | |
| 700 | 1 | |a North, Michael, |d 1964- |e editor. | |
| 776 | 0 | 8 | |i Print version: |t Sustainable catalysis, without metals or other endangered elements. Part 2. |d Cambridge, England : Royal Society of Chemistry, ©2016 |h xxv, 446 pages |k RSC green chemistry series ; 41 |x 1757-7039 |z 9781782626411 |
| 830 | 0 | |a RSC green chemistry series ; |v 41. | |
| 856 | 4 | 0 | |u https://appknovel.uam.elogim.com/kn/resources/kpSCWMOE0A/toc |z Texto completo |
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