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Asymmetric bronsted acid catalysis / / Magnus Rueping, Dixit Parmar, and Erli Sugiono
Asymmetric bronsted acid catalysis / / Magnus Rueping, Dixit Parmar, and Erli Sugiono
Autore Rueping Magnus
Edizione [1st ed.]
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2016
Descrizione fisica 1 online resource (303 pages)
Disciplina 541.395
Soggetto topico Catalysis
Asymmetric synthesis
ISBN 3-527-69479-X
3-527-69478-1
3-527-69477-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Title Page -- Copyright -- Contents -- Preface -- Chapter 1 Introduction -- 1.1 Book Structure and Notation -- 1.2 Catalyst Preparation -- 1.3 Metal Impurities -- References -- Chapter 2 Reactions of Imines -- 2.1 Nucleophilic Addition Reactions -- 2.1.1 C-Nucleophiles -- 2.1.2 N-Nucleophiles -- 2.1.3 O-Nucleophiles -- 2.1.4 P-Nucleophiles -- 2.2 Mannich Reactions -- 2.3 Strecker Reactions -- 2.4 Biginelli Reactions -- 2.5 Friedel-Crafts Reactions -- 2.5.1 Indole Coupling Partners with Aldimines -- 2.5.2 Indole Coupling Partners to Ketimines -- 2.5.3 Non-Indole Aromatic Partners -- 2.5.4 Pictet-Spengler Reactions -- 2.6 Transfer Hydrogenations -- 2.6.1 Imine Partners -- 2.6.2 α-Imino Ester Partners -- 2.6.3 N-Heterocycles -- 2.6.4 Cascade Processes -- 2.6.5 Miscellaneous Reactions -- 2.7 Pericyclic Reactions -- 2.7.1 Aza-Diels-Alder/Povarov -- 2.7.2 1,3-Dipolar Cycloaddition -- 2.7.3 Electrocyclizations and Sigmatropic Rearrangements -- 2.8 Radical Reactions -- References -- Chapter 3 Reactions of Generated Imine Intermediates -- 3.1 Enamines -- 3.1.1 Nucleophilic Addition Reactions -- 3.1.2 Transfer Hydrogenation -- 3.2 Indoles Containing Leaving Groups -- 3.2.1 Nucleophilic Addition Reactions -- 3.2.2 Friedel-Crafts Reactions -- 3.3 N-Acetals and Aminals -- 3.3.1 Nucleophilic Addition Reactions -- 3.3.2 Friedel-Crafts Reactions -- 3.3.3 Transfer Hydrogenation -- 3.4 Miscellaneous Formation -- References -- Chapter 4 Reactions of Carbonyls -- 4.1 Nucleophilic Addition Reactions -- 4.1.1 C-Nucleophiles -- 4.1.2 N-, O-, and P-Nucleophiles -- 4.2 Aldol Reactions -- 4.3 Pericyclic Reactions -- 4.4 Reductions -- References -- Chapter 5 Reactions of Generated Carbonyl Intermediates -- 5.1 Enol Ethers -- 5.2 Acetals -- 5.3 Phenols Containing Leaving Groups -- References -- Chapter 6 Reactions of Alkenes -- 6.1 Nucleophilic Addition Reactions.
6.2 Friedel-Crafts Reactions -- 6.3 Pericyclic Reactions -- 6.4 Cascades -- References -- Chapter 7 Reactions of Other Substrates -- 7.1 Aziridines -- 7.2 O-Heterocycles and Ethers -- 7.3 Hydrazines and Hydrazones -- 7.4 Azo/Diazo Substrates -- 7.5 Halogens -- 7.5.1 Fluorine -- 7.5.2 Bromine -- 7.6 Oxidizing Agents -- 7.7 Miscellaneous Substrates -- References -- Experimental Protocols -- Appendix A: Catalyst Frequency -- Appendix B: Overview of Phosphoric Acids (PA) -- Appendix C: Overview of N-Phosphoramide Acids (NPA) -- Appendix D: Overview of SPINOL Phosphoric Acids (SPA) -- Appendix E: Overview of All Other Brønsted Acids (BA) -- Index -- EULA.
Record Nr. UNINA-9910137225903321
Rueping Magnus  
Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Asymmetric bronsted acid catalysis / / Magnus Rueping, Dixit Parmar, and Erli Sugiono
Asymmetric bronsted acid catalysis / / Magnus Rueping, Dixit Parmar, and Erli Sugiono
Autore Rueping Magnus
Edizione [1st ed.]
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2016
Descrizione fisica 1 online resource (303 pages)
Disciplina 541.395
Soggetto topico Catalysis
Asymmetric synthesis
ISBN 3-527-69479-X
3-527-69478-1
3-527-69477-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Title Page -- Copyright -- Contents -- Preface -- Chapter 1 Introduction -- 1.1 Book Structure and Notation -- 1.2 Catalyst Preparation -- 1.3 Metal Impurities -- References -- Chapter 2 Reactions of Imines -- 2.1 Nucleophilic Addition Reactions -- 2.1.1 C-Nucleophiles -- 2.1.2 N-Nucleophiles -- 2.1.3 O-Nucleophiles -- 2.1.4 P-Nucleophiles -- 2.2 Mannich Reactions -- 2.3 Strecker Reactions -- 2.4 Biginelli Reactions -- 2.5 Friedel-Crafts Reactions -- 2.5.1 Indole Coupling Partners with Aldimines -- 2.5.2 Indole Coupling Partners to Ketimines -- 2.5.3 Non-Indole Aromatic Partners -- 2.5.4 Pictet-Spengler Reactions -- 2.6 Transfer Hydrogenations -- 2.6.1 Imine Partners -- 2.6.2 α-Imino Ester Partners -- 2.6.3 N-Heterocycles -- 2.6.4 Cascade Processes -- 2.6.5 Miscellaneous Reactions -- 2.7 Pericyclic Reactions -- 2.7.1 Aza-Diels-Alder/Povarov -- 2.7.2 1,3-Dipolar Cycloaddition -- 2.7.3 Electrocyclizations and Sigmatropic Rearrangements -- 2.8 Radical Reactions -- References -- Chapter 3 Reactions of Generated Imine Intermediates -- 3.1 Enamines -- 3.1.1 Nucleophilic Addition Reactions -- 3.1.2 Transfer Hydrogenation -- 3.2 Indoles Containing Leaving Groups -- 3.2.1 Nucleophilic Addition Reactions -- 3.2.2 Friedel-Crafts Reactions -- 3.3 N-Acetals and Aminals -- 3.3.1 Nucleophilic Addition Reactions -- 3.3.2 Friedel-Crafts Reactions -- 3.3.3 Transfer Hydrogenation -- 3.4 Miscellaneous Formation -- References -- Chapter 4 Reactions of Carbonyls -- 4.1 Nucleophilic Addition Reactions -- 4.1.1 C-Nucleophiles -- 4.1.2 N-, O-, and P-Nucleophiles -- 4.2 Aldol Reactions -- 4.3 Pericyclic Reactions -- 4.4 Reductions -- References -- Chapter 5 Reactions of Generated Carbonyl Intermediates -- 5.1 Enol Ethers -- 5.2 Acetals -- 5.3 Phenols Containing Leaving Groups -- References -- Chapter 6 Reactions of Alkenes -- 6.1 Nucleophilic Addition Reactions.
6.2 Friedel-Crafts Reactions -- 6.3 Pericyclic Reactions -- 6.4 Cascades -- References -- Chapter 7 Reactions of Other Substrates -- 7.1 Aziridines -- 7.2 O-Heterocycles and Ethers -- 7.3 Hydrazines and Hydrazones -- 7.4 Azo/Diazo Substrates -- 7.5 Halogens -- 7.5.1 Fluorine -- 7.5.2 Bromine -- 7.6 Oxidizing Agents -- 7.7 Miscellaneous Substrates -- References -- Experimental Protocols -- Appendix A: Catalyst Frequency -- Appendix B: Overview of Phosphoric Acids (PA) -- Appendix C: Overview of N-Phosphoramide Acids (NPA) -- Appendix D: Overview of SPINOL Phosphoric Acids (SPA) -- Appendix E: Overview of All Other Brønsted Acids (BA) -- Index -- EULA.
Record Nr. UNINA-9910830359603321
Rueping Magnus  
Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui