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Multicomponent reactions in organic synthesis /
Comprehensive and up-to-date, this book focuses on the latest advances in the field, such as newly developed techniques, more environmentally benign processes, broadened scopes, and completely novel MCRs. In addition to carbene-promoted MCRs and frequently applied metal-catalyzed MCRs, it also cover...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | , , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Weinheim, Germany :
Wiley,
©2015.
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| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 245 | 0 | 0 | |a Multicomponent reactions in organic synthesis / |c edited by Jieping Zhu, Qian Wang, Mei-Xiang Wang. |
| 260 | |a Weinheim, Germany : |b Wiley, |c ©2015. | ||
| 300 | |a 1 online resource : |b illustrations (some color) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 504 | |a Includes bibliographical references and index. | ||
| 505 | 0 | |6 880-01 |a Multicomponent Reactions in Organic Synthesis; Contents; List of Contributors; Preface; 1. General Introduction to MCRs: Past, Present, and Future; 1.1 Introduction; 1.2 Advances in Chemistry; 1.3 Total Syntheses; 1.4 Applications in Pharmaceutical and Agrochemical Industry; 1.5 Materials; 1.6 Outlook; References; 2. Discovery of MCRs; 2.1 General Introduction; 2.2 The Concept; 2.3 The Reaction Design Concept; 2.3.1 Single Reactant Replacement; 2.3.2 Modular Reaction Sequences; 2.3.3 Condition-Based Divergence; 2.3.4 Union of MCRs; 2.4 Multicomponent Reactions and Biocatalysis. | |
| 505 | 8 | |a 2.4.1 Multicomponent Reactions and (Dynamic) Enzymatic Kinetic Resolution2.4.2 Multicomponent Reactions and Enzymatic Desymmetrization; 2.5 Multicomponent Reactions in Green Pharmaceutical Production; 2.6 Conclusions; Acknowledgments; References; 3. Aryne-Based Multicomponent Reactions; 3.1 Introduction; 3.2 Multicomponent Reactions of Arynes via Electrophilic Coupling; 3.2.1 Multicomponent Reactions under Neutral Conditions; 3.2.1.1 Isocyanide-Based Multicomponent Reactions; 3.2.1.2 Imine-Based Multicomponent Reactions; 3.2.1.3 Amine-Based Multicomponent Reactions. | |
| 505 | 8 | |a 4.2.1 Phenols and Thiophenols4.2.2 Six-Membered Ring Hydroxy Heteroaromatics and Related Mercaptans; 4.2.3 Five-Membered Ring Hydroxy Heteroaromatic and Related Mercaptans; 4.2.4 Related Couplings with Enol Derivatives; 4.2.5 The Joullié-Smiles Coupling; 4.2.6 The Passerini-Smiles Reaction; 4.3 Ugi-Smiles Postcondensations; 4.3.1 Postcondensations Involving Reduction of the Nitro Group; 4.3.2 Transformations of Ugi-Smiles Thioamides; 4.3.3 Postcondensations Involving Transition Metal-Catalyzed Processes; 4.3.4 Reactivity of the Peptidyl Unit; 4.3.5 Radical Reactions; 4.3.6 Cycloaddition. | |
| 505 | 8 | |a 4.4 ConclusionsReferences; 5. 1,3-Dicarbonyls in Multicomponent Reactions; 5.1 Introduction; 5.2 Achiral and Racemic MCRs; 5.2.1 Involving One Pronucleophilic Reactive Site; 5.2.2 Involving Two Reactive Sites; 5.2.2.1 Two Nucleophilic Sites; 5.2.2.2 One Pronucleophilic Site and One Electrophilic Site; 5.2.3 Involving Three Reactive Sites; 5.2.4 Involving Four Reactive Sites; 5.3 Enantioselective MCRs; 5.3.1 Involving One Reactive Site; 5.3.2 Involving Two Reactive Sites; 5.3.3 Involving Three Reactive Sites; 5.4 Conclusions and Outlook; References; 6. Functionalization of Heterocycles by MCRs. | |
| 520 | |a Comprehensive and up-to-date, this book focuses on the latest advances in the field, such as newly developed techniques, more environmentally benign processes, broadened scopes, and completely novel MCRs. In addition to carbene-promoted MCRs and frequently applied metal-catalyzed MCRs, it also covers recently developed catalytic enantioselective variants as well as MCR in drug discovery and for the synthesis of heterocyclic molecules and macrocycles. Edited by the leading experts and with a list of authors reading like a ""who's who"" in multicomponent reaction chemistry, this is definitely a | ||
| 590 | |a ProQuest Ebook Central |b Ebook Central Academic Complete | ||
| 650 | 0 | |a Organic compounds |x Synthesis. | |
| 650 | 6 | |a Composés organiques |x Synthèse. | |
| 650 | 7 | |a SCIENCE |x Chemistry |x Organic. |2 bisacsh | |
| 650 | 7 | |a Organic compounds |x Synthesis |2 fast | |
| 700 | 1 | |a Zhu, Jieping. | |
| 700 | 1 | |a Wang, Qian |c (Research scientist) |1 https://id.oclc.org/worldcat/entity/E39PCjFDC4R8XxPmKrk6fhqwBX | |
| 700 | 1 | |a Wang, Mei-Xiang. | |
| 758 | |i has work: |a Multicomponent reactions in organic synthesis (Text) |1 https://id.oclc.org/worldcat/entity/E39PCGxjTBwCrppYbTpKWW6ywK |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
| 776 | 0 | 8 | |i Print version: |a Zhu, Jieping. |t Multicomponent Reactions in Organic Synthesis. |d Hoboken : Wiley, ©2014 |z 9783527332373 |
| 856 | 4 | 0 | |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=1818244 |z Texto completo |
| 880 | 0 | 0 | |6 505-00/(S |g Machine generated contents note: |g 1.1. |t Introduction / |r AlAnod D. AlQahtani / |r Alexander Dömling -- |g 1.2. |t Advances in Chemistry / |r AlAnod D. AlQahtani / |r Alexander Dömling -- |g 1.3. |t Total Syntheses / |r AlAnod D. AlQahtani / |r Alexander Dömling -- |g 1.4. |t Applications in Pharmaceutical and Agrochemical Industry / |r AlAnod D. AlQahtani / |r Alexander Dömling -- |g 1.5. |t Materials / |r AlAnod D. AlQahtani / |r Alexander Dömling -- |g 1.6. |t Outlook / |r AlAnod D. AlQahtani / |r Alexander Dömling -- |t References / |r AlAnod D. AlQahtani / |r Alexander Dömling -- |g 2.1. |t General Introduction / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.2. |t Concept / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.3. |t Reaction Design Concept / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.3.1. |t Single Reactant Replacement / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.3.2. |t Modular Reaction Sequences / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.3.3. |t Condition-Based Divergence / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.3.4. |t Union of MCRs / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.4. |t Multicomponent Reactions and Biocatalysis / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.4.1. |t Multicomponent Reactions and (Dynamic) Enzymatic Kinetic Resolution / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.4.2. |t Multicomponent Reactions and Enzymatic Desymmetrization / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.5. |t Multicomponent Reactions in Green Pharmaceutical Production / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 2.6. |t Conclusions / |r Romano V.A. Orru / |r Eelco Ruijter -- |t Acknowledgments / |r Romano V.A. Orru / |r Eelco Ruijter -- |t References / |r Romano V.A. Orru / |r Eelco Ruijter -- |g 3.1. |t Introduction / |r Hiroto Yoshida -- |g 3.2. |t Multicomponent Reactions of Arynes via Electrophilic Coupling / |r Hiroto Yoshida -- |g 3.2.1. |t Multicomponent Reactions under Neutral Conditions / |r Hiroto Yoshida -- |g 3.2.1.1. |t Isocyanide-Based Multicomponent Reactions / |r Hiroto Yoshida -- |g 3.2.1.2. |t Imine-Based Multicomponent Reactions / |r Hiroto Yoshida -- |g 3.2.1.3. |t Amine-Based Multicomponent Reactions / |r Hiroto Yoshida -- |g 3.2.1.4. |t Carbonyl Compound-Based Multicomponent Reactions / |r Hiroto Yoshida -- |g 3.2.1.5. |t Ether-Based Multicomponent Reactions / |r Hiroto Yoshida -- |g 3.2.1.6. |t Miscellaneous / |r Hiroto Yoshida -- |g 3.2.2. |t Multicomponent Reactions under Basic Conditions / |r Hiroto Yoshida -- |g 3.3. |t Transition Metal-Catalyzed Multicomponent Reactions of Arynes / |r Hiroto Yoshida -- |g 3.3.1. |t Annulations / |r Hiroto Yoshida -- |g 3.3.2. |t Cross-Coupling-Type Reactions / |r Hiroto Yoshida -- |g 3.3.3. |t Mizoroki-Heck-Type Reactions / |r Hiroto Yoshida -- |g 3.3.4. |t Insertion into σ-Bond / |r Hiroto Yoshida -- |g 3.4. |t Concluding Remarks / |r Hiroto Yoshida -- |t References / |r Hiroto Yoshida -- |g 4.1. |t Introduction / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.1.1. |t Carboxylic Acid Surrogates in Ugi Reactions / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.1.2. |t Smiles Rearrangements / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.2. |t Scope and Limitations / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.2.1. |t Phenols and Thiophenols / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.2.2. |t Six-Membered Ring Hydroxy Heteroaromatics and Related Mercaptans / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.2.3. |t Five-Membered Ring Hydroxy Heteroaromatic and Related Mercaptans / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.2.4. |t Related Couplings with Enol Derivatives / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.2.5. |t Joullié-Smiles Coupling / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.2.6. |t Passerini-Smiles Reaction / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.3. |t Ugi-Smiles Postcondensations / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.3.1. |t Postcondensations Involving Reduction of the Nitro Group / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.3.2. |t Transformations of Ugi-Smiles Thioamides / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.3.3. |t Postcondensations Involving Transition Metal-Catalyzed Processes / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.3.4. |t Reactivity of the Peptidyl Unit / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.3.5. |t Radical Reactions / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.3.6. |t Cycloaddition / |r Laurence Grimaud / |r Laurent El Kaim -- |g 4.4. |t Conclusions / |r Laurence Grimaud / |r Laurent El Kaim -- |t References / |r Laurence Grimaud / |r Laurent El Kaim -- |g 5.1. |t Introduction / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.2. |t Achiral and Racemic MCRs / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.2.1. |t Involving One Pronucleophilic Reactive Site / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.2.2. |t Involving Two Reactive Sites / |r Yoann Coquerel / |r Thierry Constantieux / |r Xavier Bugaut / |r Jean Rodriguez -- |g 5.2.2.1. |t Two Nucleophilic Sites / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.2.2.2. |t One Pronucleophilic Site and One Electrophilic Site / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.2.3. |t Involving Three Reactive Sites / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.2.4. |t Involving Four Reactive Sites / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.3. |t Enantioselective MCRs / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.3.1. |t Involving One Reactive Site / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.3.2. |t Involving Two Reactive Sites / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.3.3. |t Involving Three Reactive Sites / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 5.4. |t Conclusions and Outlook / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |t References / |r Xavier Bugaut / |r Jean Rodriguez / |r Yoann Coquerel / |r Thierry Constantieux -- |g 6.1. |t Introduction / |r Esther Vicente-Garcia / |r Rodolfo Lavilla / |r Nicola Kielland -- |g 6.2. |t Mannich-Type Reactions and Related Processes / |r Esther Vicente-Garcia / |r Rodolfo Lavilla / |r Nicola Kielland -- |g 6.3. |t β-Dicarbonyl Chemistry / |r Esther Vicente-Garcia / |r Rodolfo Lavilla / |r Nicola Kielland -- |g 6.4. |t Hetero-Diels[--]Alder Cycloadditions and Related Processes / |r Esther Vicente-Garcia / |r Rodolfo Lavilla / |r Nicola Kielland -- |g 6.5. |t Metal-Mediated Processes / |r Esther Vicente-Garcia / |r Rodolfo Lavilla / |r Nicola Kielland -- |g 6.6. |t Isocyanide-Based Reactions / |r Esther Vicente-Garcia / |r Rodolfo Lavilla / |r Nicola Kielland -- |g 6.7. |t Dipole-Mediated Processes / |r Esther Vicente-Garcia / |r Rodolfo Lavilla / |r Nicola Kielland -- |g 6.8. |t Conclusions / |r Nicola Kielland / |r Esther Vicente-Garcia / |r Rodolfo Lavilla -- |t Acknowledgments / |r Esther Vicente-Garcia / |r Rodolfo Lavilla / |r Nicola Kielland -- |t References / |r Esther Vicente-Garcia / |r Rodolfo Lavilla / |r Nicola Kielland -- |g 7.1. |t Introduction / |r Wenhao Hu / |r Dong Xing -- |g 7.2. |t MCRs via Carbonyl or Azomethine Ylide-Involved 1,3-Dipolar Cycloadditions / |r Wenhao Hu / |r Dong Xing -- |g 7.2.1. |t Azomethine Ylide / |r Wenhao Hu / |r Dong Xing -- |g 7.2.2. |t Carbonyl Ylide / |r Wenhao Hu / |r Dong Xing -- |g 7.3. |t MCRs via Electrophilic Trapping of Protic Onium Ylides / |r Wenhao Hu / |r Dong Xing -- |g 7.3.1. |t Initial Development / |r Wenhao Hu / |r Dong Xing -- |g 7.3.2. |t Asymmetric Examples / |r Wenhao Hu / |r Dong Xing -- |g 7.3.2.1. |t Chiral Reagent Induction / |r Wenhao Hu / |r Dong Xing -- |g 7.3.2.2. |t Chiral Dirhodium(II) Catalysis / |r Wenhao Hu / |r Dong Xing -- |g 7.3.2.3. |t Enantioselective Synergistic Catalysis / |r Dong Xing / |r Wenhao Hu -- |g 7.3.3. |t MCRs Followed by Tandem Cyclizations / |r Wenhao Hu / |r Dong Xing -- |g 7.4. |t MCRs via Electrophilic Trapping of Zwitterionic Intermediates / |r Dong Xing / |r Wenhao Hu -- |g 7.5. |t MCRs via Metal Carbene Migratory Insertion / |r Dong Xing / |r Wenhao Hu -- |g 7.6. |t Summary and Outlook / |r Dong Xing / |r Wenhao Hu -- |t References / |r Wenhao Hu / |r Dong Xing -- |g 8.1. |t Introduction / |r Fabio Lorenzini / |r Bruce A. Arndtsen / |r Jeffrey S. Quesnel / |r Jevgenijs Tjutrins -- |g 8.2. |t Multicomponent Cross-Coupling and Carbonylation Reactions / |r Fabio Lorenzini / |r Jevgenijs Tjutrins / |r Jeffrey S. Quesnel / |r Bruce A. Arndtsen -- |g 8.2.1. |t Cyclization with Alkyne- or Alkene-Containing Nucleophiles / |r Fabio Lorenzini / |r Jevgenijs Tjutrins / |r Bruce A. Arndtsen / |r Jeffrey S. Quesnel -- |g 8.2.2. |t Cyclization via Palladium[--]Allyl Complexes / |r Jeffrey S. |
| 880 | 0 | 0 | |r Quesnel / |r Fabio Lorenzini / |r Jevgenijs Tjutrins / |r Bruce A. Arndtsen -- |g 8.2.3. |t Fused-Ring Heterocycles for ortho-Substituted Arene Building Blocks / |r Fabio Lorenzini / |r Jevgenijs Tjutrins / |r Jeffrey S. Quesnel / |r Bruce A. Arndtsen -- |g 8.2.4. |t Multicomponent Cyclocarbonylations / |r Fabio Lorenzini / |r Jevgenijs Tjutrins / |r Bruce A. Arndtsen / |r Jeffrey S. Quesnel -- |g 8.2.5. |t Cyclization of Cross-Coupling Reaction Products / |r Bruce A. Arndtsen / |r Jeffrey S. Quesnel / |r Jevgenijs Tjutrins / |r Fabio Lorenzini -- |g 8.2.6. |t C[--]H Functionalization in Multicomponent Reactions / |r Jevgenijs Tjutrins / |r Bruce A. Arndtsen / |r Jeffrey S. Quesnel / |r Fabio Lorenzini -- |g 8.3. |t Metallacycles in Multicomponent Reactions / |r Jeffrey S. Quesnel / |r Bruce A. Arndtsen / |r Jevgenijs Tjutrins / |r Fabio Lorenzini -- |g 8.4. |t Multicomponent Reactions via 1,3-Dipolar Cycloaddition / |r Fabio Lorenzini / |r Jevgenijs Tjutrins / |r Jeffrey S. Quesnel / |r Bruce A. Arndtsen -- |g 8.5. |t Concluding Remarks / |r Jevgenijs Tjutrins / |r Bruce A. Arndtsen / |r Jeffrey S. Quesnel / |r Fabio Lorenzini -- |t References / |r Fabio Lorenzini / |r Jevgenijs Tjutrins / |r Jeffrey S. Quesnel / |r Bruce A. Arndtsen -- |g 9.1. |t Introduction / |r Ricardo A.W. Neves Filho / |r Micjel C. Morejon / |r Alfredo R. Puentes / |r Ludger A. Wessjohann -- |g 9.2. |t IMCR-Based Macrocyclizations of Single Bifunctional Building Blocks / |r Alfredo R. Puentes / |r Micjel C. Morejon / |r Ricardo A.W. Neves Filho / |r Ludger A. Wessjohann. |
| 880 | 0 | 0 | |6 505-01/(S |g Contents note continued: |g 9.3. |t Multiple MCR-Based Macrocyclizations of Bifunctional Building Blocks / |r Ricardo A.W. Neves Filho / |r Micjel C. Morejon / |r Alfredo R. Puentes / |r Ludger A. Wessjohann -- |g 9.4. |t IMCR-Based Macrocyclizations of Trifunctionalized Building Blocks (MiB-3D) / |r Alfredo R. Puentes / |r Micjel C. Morejon / |r Ricardo A.W. Neves Filho / |r Ludger A. Wessjohann -- |g 9.5. |t Sequential IMCR-Based Macrocyclizations of Multiple Bifunctional Building Blocks / |r Ricardo A.W. Neves Filho / |r Alfredo R. Puentes / |r Micjel C. Morejon / |r Ludger A. Wessjohann -- |g 9.6. |t Final Remarks and Future Perspectives / |r Ricardo A.W. Neves Filho / |r Ludger A. Wessjohann / |r Alfredo R. Puentes / |r Micjel C. Morejon -- |t References / |r Ludger A. Wessjohann / |r Ricardo A.W. Neves Filho / |r Alfredo R. Puentes / |r Micjel C. Morejon -- |g 10.1. |t Introduction / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.2. |t Multicomponent Reactions Involving In Situ Oxidation of One Substrate / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.2.1. |t Isocyanide-Based Multicomponent Reactions / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.2.1.1. |t Passerini Reactions / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.2.1.2. |t Ugi Reactions with In Situ Oxidation of Alcohols / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.2.1.3. |t Ugi Reaction with In Situ Oxidation of Secondary Amines / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.2.1.4. |t Ugi[--]Smiles Reaction with In Situ Oxidation of Secondary Amines / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.2.1.5. |t Ugi-Type Reactions by In Situ Oxidation of Tertiary Amines / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.2.1.6. |t Synthesis of Other Derivatives / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.2.2. |t Other Multicomponent Reactions / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.3. |t Multicomponent Reactions Involving Oxidation of a Reaction Intermediate / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.3.1. |t Reactions without Transition Metal-Mediated Oxidation / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.3.2. |t Reactions Mediated by Transition Metal Catalysis / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.4. |t Multicomponent Reactions Involving Oxidants as Lewis Acids / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 10.5. |t Conclusions / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |t References / |r Andrea Basso / |r Renata Riva / |r Lisa Moni -- |g 11.1. |t Introduction / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 11.2. |t Reactions with 1,2-Propadiene and Unactivated Allenes / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 11.2.1. |t Palladium-Catalyzed Multicomponent Reactions / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 11.2.2. |t Copper-, Nickel-, and Rhodium-Promoted Multicomponent Reactions / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 11.2.3. |t Multicomponent Reactions without Transition Metals / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 11.3. |t Reactions with Acceptor-Substituted Allenes / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 11.3.1. |t Catalyzed Multicomponent Reactions / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 11.3.2. |t Uncatalyzed Multicomponent Reactions / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 11.4. |t Reactions with Donor-Substituted Allenes / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 11.5. |t Conclusions / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |t List of Abbreviations / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |t References / |r Reinhold Zimmer / |r Hans-Ulrich Reissig -- |g 12.1. |t Introduction / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.2. |t σ-Nucleophilic Reactivity of Alkynes / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.2.1. |t Acetylide Additions to Electrophiles / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.2.1.1. |t Alkyne[--]Aldehyde[--]Amine Condensation [--] A3-Coupling / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.2.1.2. |t Alkyne[--](Hetero)Aryl Halide (Sonogashira) Coupling as Key Reaction / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.2.2. |t Conversion of Terminal Alkynes into Electrophiles as Key Reactions / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.3. |t π-Nucleophilic Reactivity of Alkynes / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.4. |t Alkynes as Electrophilic Partners / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.5. |t Alkynes in Cycloadditions / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.5.1. |t Alkynes as Dipolarophiles / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.5.2. |t Alkynes in Cu(I)-Catalyzed 1,3-Dipolar Azide[--]Alkyne Cycloaddition / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.5.3. |t Alkynes as Dienophiles in MCRs / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.6. |t Alkynes as Reaction Partners in Organometallic MCRs / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 12.7. |t Conclusions / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |t List of Abbreviations / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |t Acknowledgment / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |t References / |r Konstantin Deilhof / |r Thomas J.J. Müller -- |g 13.1. |t Introduction / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.2. |t Quinolones and Related Heterocycles from Homophthalic and Isatoic Anhydrides / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.2.1. |t Introduction: Reactivity of Homophthalic and Isatoic Anhydrides / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.2.2. |t Imine[--]Anhydride Reactions of Homophthalic Anhydride / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.2.3. |t MCRs Employing Homophthalic Anhydride / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.2.4. |t Imine[--]Anhydride Reactions of Isatoic Anhydride / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.3. |t α, β-Unsaturated Cyclic Anhydrides: MCRs Involving Conjugate Addition and Cycloaddition Reactions / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.3.1. |t Maleic Anhydride MCRs / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.3.2. |t MCRs of Itaconic Anhydrides / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.3.3. |t Diels[--]Alder Reactions / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.4. |t MCRs of Cyclic Anhydrides in Annulation Reactions and Related Processes / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.4.1. |t MCR-Based Annulations: Succinic and Phthalic Anhydrides / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.5. |t MCRs of Acyclic Anhydrides / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |g 13.6. |t Conclusions / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. Shaw -- |t References / |r Kevin S. Martin / |r Ashkaan Younai / |r Jared T. |
| 880 | 0 | 0 | |t Shaw -- |g 14.1. |t Introduction / |r Yannick Landais / |r Virginie Liautard -- |g 14.2. |t MCRs Involving Addition Across Olefin C=C Bonds / |r Yannick Landais / |r Virginie Liautard -- |g 14.2.1. |t Addition of Aryl Radicals to Olefins / |r Yannick Landais / |r Virginie Liautard -- |g 14.2.2. |t MCRs Using Sulfonyl Derivatives as Terminal Trap / |r Yannick Landais / |r Virginie Liautard -- |g 14.2.3. |t Carboallylation of Electron-Poor Olefins / |r Yannick Landais / |r Virginie Liautard -- |g 14.2.4. |t Carbohydroxylation, Sulfenylation, and Phosphorylation of Olefins / |r Yannick Landais / |r Virginie Liautard -- |g 14.2.5. |t Radical Addition to Olefins Using Photoredox Catalysis / |r Yannick Landais / |r Virginie Liautard -- |g 14.2.6. |t MCRs Based on Radical[--]Polar Crossover Processes / |r Yannick Landais / |r Virginie Liautard -- |g 14.3. |t Free-Radical Carbonylation / |r Virginie Liautard / |r Yannick Landais -- |g 14.3.1. |t Alkyl Halide Carbonylation / |r Yannick Landais / |r Virginie Liautard -- |g 14.3.2. |t Metal-Mediated Atom-Transfer Radical Carbonylation / |r Virginie Liautard / |r Yannick Landais -- |g 14.3.3. |t Alkane Carbonylation / |r Virginie Liautard / |r Yannick Landais -- |g 14.3.4. |t Miscellaneous Carbonylation Reactions / |r Virginie Liautard / |r Yannick Landais -- |g 14.4. |t Free-Radical Oxygenation / |r Virginie Liautard / |r Yannick Landais -- |g 14.5. |t MCRs Involving Addition Across π-C=N Bonds / |r Yannick Landais / |r Virginie Liautard -- |g 14.5.1. |t Free-Radical Strecker Process / |r Virginie Liautard / |r Yannick Landais -- |g 14.5.2. |t Free-Radical Mannich-Type Processes / |r Yannick Landais / |r Virginie Liautard -- |g 14.6. |t Miscellaneous Free-Radical Multicomponent Reactions / |r Virginie Liautard / |r Yannick Landais -- |g 14.7. |t Conclusions / |r Virginie Liautard / |r Yannick Landais -- |t References / |r Virginie Liautard / |r Yannick Landais -- |g 15.1. |t Introduction / |r Xiang Wu / |r Liu-Zhu Gong -- |g 15.2. |t Mannich Reaction / |r Liu-Zhu Gong / |r Xiang Wu -- |g 15.3. |t Ugi-Type Reaction / |r Xiang Wu / |r Liu-Zhu Gong -- |g 15.4. |t Biginelli Reaction / |r Liu-Zhu Gong / |r Xiang Wu -- |g 15.5. |t Aza-Diels[--]Alder Reaction / |r Xiang Wu / |r Liu-Zhu Gong -- |g 15.6. |t 1,3-Dipolar Cycloaddition / |r Liu-Zhu Gong / |r Xiang Wu -- |g 15.7. |t Hantzsch Dihydropyridine Synthesis / |r Xiang Wu / |r Liu-Zhu Gong -- |g 15.8. |t Combination of Metal and Chiral Phosphoric Acid for Multicomponent Reaction / |r Liu-Zhu Gong / |r Xiang Wu -- |g 15.9. |t Other Phosphoric Acid-Catalyzed Multicomponent Reactions / |r Xiang Wu / |r Liu-Zhu Gong -- |g 15.10. |t Summary / |r Liu-Zhu Gong / |r Xiang Wu -- |t References / |r Xiang Wu / |r Liu-Zhu Gong. |
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