Jie Jack Li
Name Reactions in Heterocyclic Chemistry II (eBook, PDF)
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Jie Jack Li
Name Reactions in Heterocyclic Chemistry II (eBook, PDF)
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The up-to-DATE guide to name reactions in heterocyclic chemistry Name Reactions in Heterocyclic Chemistry II presents a comprehensive treatise on name reactions in heterocyclic chemistry, one of the most exciting--and important--fields within organic chemistry today. The book not only covers fresh ground, but also provides extensive information on new and/or expanded reactions in: * Three- and four-membered heterocycles * Five-membered heterocycles (pyrroles and pyrrolidines, indoles, furans, thiophenes, and oxazoles) * Six-membered heterocycles, including pyridines, quinolines, and…mehr
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The up-to-DATE guide to name reactions in heterocyclic chemistry Name Reactions in Heterocyclic Chemistry II presents a comprehensive treatise on name reactions in heterocyclic chemistry, one of the most exciting--and important--fields within organic chemistry today. The book not only covers fresh ground, but also provides extensive information on new and/or expanded reactions in: * Three- and four-membered heterocycles * Five-membered heterocycles (pyrroles and pyrrolidines, indoles, furans, thiophenes, and oxazoles) * Six-membered heterocycles, including pyridines, quinolines, and isoquinolines Featuring contributions from the leading authorities in heterocyclic chemistry. Each section includes a description of the given reaction, as well as the relevant historical perspective, mechanism, variations and improvements, synthetic utilities, experimental details, and references to the current primary literature. The reactions covered in Name Reactions in Heterocyclic Chemistry have been widely adopted in all areas of organic synthesis, from the medicinal/pharmaceutical field, to agriculture, to fine chemicals, and the book brings the most cutting-edge knowledge to practicing synthetic chemists and students, along with the tools needed to synthesize new and useful molecules.
Produktdetails
- Produktdetails
- Verlag: John Wiley & Sons
- Seitenzahl: 704
- Erscheinungstermin: 28. September 2011
- Englisch
- ISBN-13: 9781118092859
- Artikelnr.: 37486541
- Verlag: John Wiley & Sons
- Seitenzahl: 704
- Erscheinungstermin: 28. September 2011
- Englisch
- ISBN-13: 9781118092859
- Artikelnr.: 37486541
Jie Jack Li is a Chemist at Bristol-Myers Squibb Company. He has authored or edited various books, including the first volume of Name Reactions in Heterocyclic Chemistry, Name Reactions for Functional Group Transformations, Name Reactions for Carbocyclic Ring Formations, and several others, all published by Wiley.
Foreword viii Preface ix Contributing Authors xi Part 1 Three- and Four-Membered Heterocycles 1 Chapter 1 Aziridines and Epoxides 1 1.1 Blum Aziridine Synthesis 2 1.2 Gabriel-Heine Aziridine Isomerization 11 1.3 Shi Epoxidation 21 Part 2 Five-Membered Heterocycles 41 Chapter 2 Pyrroles and Pyrrolidines 41 2.1 Clauson-Kass Pyrrole Synthesis 42 2.2 Houben-Hoesch Acylation of Pyrroles 53 2.3 Overman Pyrrolidine Synthesis 60 2.4 Trofimov Synthesis of Pyrroles 72 Chapter 3 Indoles 83 3.1 Bischler-Möhlau Indole Synthesis 84 3.2 Borsche-Drechsel Cyclization 91 3.3 Buchwald-Hartwig Indole Synthesis 102 3 .4 Cadogan-Sundberg Indole Synthesis 112 3.5 Fukuyama Indole Synthesis 125 3.6 Gassman Oxindole Synthesis 133 3.7 Larock Indole Synthesis 143 3.8 Matinet Dioxindole Reaction 167 3.9 Mori-Ban Indole Synthesis 175 3.10 Sandmeyer Isatin Synthesis 187 3.11 Sommelet-Hauser Rearrangement 197 3.12 Stolle Oxindole Synthesis 207 Chapter 4 Furans and Ox azoles 213 4.1 Nierenstein Reaction 214 4.2 Davidson Oxazole Synthesis 221 4.3 Fischer Oxazole Synthesis 225 4.4 Japp Oxazole Synthesis 233 4.5 Schhllkopf Oxazole Synthesis 242 Chapter 5 Other Five-Mem be red Heterocycles 259 5. L Bamberger Imidazole Cleavage 260 5.2 Dimroth Triazole Synthesis 269 5.3 Finnegan Tetrazole Synthesis 278 5.4 Hantzsch Thiazole Synthesis 299 5.5 Huisgen Tetrazole Rearrangement 309 5.6 Knorr Pyrazole Synthesis 317 5.7 Pechmann Pyrazole Synthesis 327 Part 3 Six-Membered Heterocycles 337 Chapter 6 Pyridincs 337 6.1 Baeyer Pyridine Synthesis 338 6.2 Katrizky Pyridine Synthesis 347 Chapter 7 Quinolines and Isoquinolines 351 7.1 Betti Reaction 352 7.2 Bemthsen Acridine Synthesis 360 7.3 Lehmstedt-Tanasescu Reaction 368 7.4 Niementowski Quinoline Synthesis 376 7.5 Povarov Reaction 385 Chapter 8 Six-Membered Heterocycles 401 8.1 Balaban-Nenitzescu-Praill Reaction 402 8.2 Borsche Cinnoline Synthesis 420 8.3 Gutknecht Pyrazine Synthesis 430 8.4 Niementowski Quinazoline Synthesis 440 8.5 Pechmann Coumarin Synthesis 454 8.6 Robin son-Schöpf Condensation 470 8.7 Simonis Chromone Cyclization 477 8.8 Wesseley--Moser Rearrangement 487 8.9 Widman-Stoermer Cinnoline Synthesis 493 8.10 Wichterle Reaction 497 Chapter 9 Miscellaneous Name Reactions 515 9.1 ANRORC Mechanism 516 9.2 Boulton-Katritzky Rearrangement 527 9.3 Chichibabin Animation Reaction 539 9.4 Dimroth Rearrangement 554 9.5 Hantzsch Synthesis 591 9.6 Ortolcva-King Reaction 645 Appendixes Appendix 1, Table of Contents for Volume 1: Name Reactions in Heterocyclic Chemistry 651 Appendix 2, Table of Contents for Volume 2: Name Reactions for Functional Group Transformations 655 Appendix 3, Table of Contents for Volume 3: Name Reactions for Hornolegations-I 657 Appendix 4, Table of Contents for Volume 4; Name Reactions for Hornohgations-II 659 Appendix 5, Table of Contents for Volume 5: Name Reactions for Ring Formations 661 Subject Index 663
Foreword. Preface. Contributing Authors. PART 1 THREE- AND FOUR-MEMBERED
HETEROCYCLES. Chapter 1 Aziridines and Epoxides. 1.1 Blum Aziridine
Synthesis. 1.2 Gabriel-Heine Aziridine Isomerization. 1.3 Shi Epoxidation.
PART 2 FIVE-MEMBERED HETEROCYCLES. Chapter 2 Pyrroles and Pyrrolidines. 2.1
Clauson-Kass Pyrrole Synthesis. 2.2 Houben-Hoech Acylation of Pyrroles. 2.3
Overman Pyrrolidine Synthesis. 2.4 Trofimov Synthesis of Pyrroles. Chapter
3 Indoles. 3.1 Bischler-Möhlau Indole Synthesis. 3.2 Borsche-Drechsel
Cyclization. 3.3 Buchwald-Hartwig Indole Synthesis. 3.4 Cadogan-Sundberg
Indole Synthesis. 3.5 Fukuyama Indole Synthesis. 3.6 Gassman Oxindole
Synthesis. 3.7 Larock Indole Synthesis. 3.8 Matinet Dioxindole Synthesis.
3.9 Mori-Ban Indole Synthesis. 3.10 Sandmeyer Isatin Synthesis. 3.11
Sommelet-Hauser Rearrangement. 3.12 Stollé Oxindole Synthesis. Chapter 4
Furans and Oxazoles. 4.1 Nierenstein Reaction. 4.2 Davidson Oxazole
Synthesis. 4.3 Fischer Oxazole Synthesis. 4.4 Japp Oxazole Synthesis. 4.5
Schöllkopf Oxazole Synthesis. Chapter 5 Other Five-Membered Heterocycles.
5.1 Bamberger Imidazole Cleavage. 5.2 Dimroth Triazole Synthesis. 5.3
Finnegan Tetrazole Synthesis. 5.4 Hantsch Thiazole Synthesis. 5.5 Huisgen
Tetrazole Rearrangement. 5.6 Knorr Pyrazole Synthesis. 5.7 Pechmann
Pyrazole Synthesis. PART 3 SIX-MEMBERED HETEROCYCLES. Chapter 6 Pyridines.
6.1 Baeyer Pyridine Synthesis. 6.2 Katrizky Reaction. Chapter 7 Quinolines
and Isoquinolines. 7.1 Betti reaction. 7.2 Bernthsen Acridine Synthesis.
7.3 Lehmstedt-Tanasescu Reaction. 7.4 Niementowski Quinoline Synthesis. 7.5
Povarov Reaction. Chapter 8 Six-Membered Heterocycles. 8.1
Balaban-Nenitzescu-Praill Reaction. 8.2 Borsche Cinnoline Synthesis. 8.3
Gutknecht Pyrazine Synthesis. 8.4 Niementowski Quinazoline Synthesis. 8.5
Pechmann Coumarin Synthesis. 8.6 Robinson-Schöpf Condensation. 8.7 Simonis
Chromone Cyclization. 8.8 Wesseley-Moser Rearrangement. 8.9 Widman-Stoermer
Cinnoline Synthesis. 8.10 Wichterle Reaction. Chapter 9 Miscellaneous Name
Reactions. 9.1 ANRORC Mechanism. 9.2 Boulton-Katritzky Rearrangement. 9.3
Chichibabin Amination Reaction. 9.4 Dimroth Rearrangement. 9.5 Hantzsch
Synthesis. 9.6 Ortoleva-King Reaction. Appendices. Appendix 1, Table of
Contents for Volume 1: Name Reactions in Heterocyclic Chemistry. Appendix
2, Table of Contents for Volume 2: Name Reactions for Functional Group
Transformations. Appendix 3, Table of Contents for Volume 3: Name Reactions
for Homologations-I. Appendix 4, Table of Contents for Volume 4: Name
Reactions for Homologations-II. Appendix 5, Table of Contents for Volume 5:
Name Reactions for Ring Formations.
HETEROCYCLES. Chapter 1 Aziridines and Epoxides. 1.1 Blum Aziridine
Synthesis. 1.2 Gabriel-Heine Aziridine Isomerization. 1.3 Shi Epoxidation.
PART 2 FIVE-MEMBERED HETEROCYCLES. Chapter 2 Pyrroles and Pyrrolidines. 2.1
Clauson-Kass Pyrrole Synthesis. 2.2 Houben-Hoech Acylation of Pyrroles. 2.3
Overman Pyrrolidine Synthesis. 2.4 Trofimov Synthesis of Pyrroles. Chapter
3 Indoles. 3.1 Bischler-Möhlau Indole Synthesis. 3.2 Borsche-Drechsel
Cyclization. 3.3 Buchwald-Hartwig Indole Synthesis. 3.4 Cadogan-Sundberg
Indole Synthesis. 3.5 Fukuyama Indole Synthesis. 3.6 Gassman Oxindole
Synthesis. 3.7 Larock Indole Synthesis. 3.8 Matinet Dioxindole Synthesis.
3.9 Mori-Ban Indole Synthesis. 3.10 Sandmeyer Isatin Synthesis. 3.11
Sommelet-Hauser Rearrangement. 3.12 Stollé Oxindole Synthesis. Chapter 4
Furans and Oxazoles. 4.1 Nierenstein Reaction. 4.2 Davidson Oxazole
Synthesis. 4.3 Fischer Oxazole Synthesis. 4.4 Japp Oxazole Synthesis. 4.5
Schöllkopf Oxazole Synthesis. Chapter 5 Other Five-Membered Heterocycles.
5.1 Bamberger Imidazole Cleavage. 5.2 Dimroth Triazole Synthesis. 5.3
Finnegan Tetrazole Synthesis. 5.4 Hantsch Thiazole Synthesis. 5.5 Huisgen
Tetrazole Rearrangement. 5.6 Knorr Pyrazole Synthesis. 5.7 Pechmann
Pyrazole Synthesis. PART 3 SIX-MEMBERED HETEROCYCLES. Chapter 6 Pyridines.
6.1 Baeyer Pyridine Synthesis. 6.2 Katrizky Reaction. Chapter 7 Quinolines
and Isoquinolines. 7.1 Betti reaction. 7.2 Bernthsen Acridine Synthesis.
7.3 Lehmstedt-Tanasescu Reaction. 7.4 Niementowski Quinoline Synthesis. 7.5
Povarov Reaction. Chapter 8 Six-Membered Heterocycles. 8.1
Balaban-Nenitzescu-Praill Reaction. 8.2 Borsche Cinnoline Synthesis. 8.3
Gutknecht Pyrazine Synthesis. 8.4 Niementowski Quinazoline Synthesis. 8.5
Pechmann Coumarin Synthesis. 8.6 Robinson-Schöpf Condensation. 8.7 Simonis
Chromone Cyclization. 8.8 Wesseley-Moser Rearrangement. 8.9 Widman-Stoermer
Cinnoline Synthesis. 8.10 Wichterle Reaction. Chapter 9 Miscellaneous Name
Reactions. 9.1 ANRORC Mechanism. 9.2 Boulton-Katritzky Rearrangement. 9.3
Chichibabin Amination Reaction. 9.4 Dimroth Rearrangement. 9.5 Hantzsch
Synthesis. 9.6 Ortoleva-King Reaction. Appendices. Appendix 1, Table of
Contents for Volume 1: Name Reactions in Heterocyclic Chemistry. Appendix
2, Table of Contents for Volume 2: Name Reactions for Functional Group
Transformations. Appendix 3, Table of Contents for Volume 3: Name Reactions
for Homologations-I. Appendix 4, Table of Contents for Volume 4: Name
Reactions for Homologations-II. Appendix 5, Table of Contents for Volume 5:
Name Reactions for Ring Formations.
Foreword viii Preface ix Contributing Authors xi Part 1 Three- and Four-Membered Heterocycles 1 Chapter 1 Aziridines and Epoxides 1 1.1 Blum Aziridine Synthesis 2 1.2 Gabriel-Heine Aziridine Isomerization 11 1.3 Shi Epoxidation 21 Part 2 Five-Membered Heterocycles 41 Chapter 2 Pyrroles and Pyrrolidines 41 2.1 Clauson-Kass Pyrrole Synthesis 42 2.2 Houben-Hoesch Acylation of Pyrroles 53 2.3 Overman Pyrrolidine Synthesis 60 2.4 Trofimov Synthesis of Pyrroles 72 Chapter 3 Indoles 83 3.1 Bischler-Möhlau Indole Synthesis 84 3.2 Borsche-Drechsel Cyclization 91 3.3 Buchwald-Hartwig Indole Synthesis 102 3 .4 Cadogan-Sundberg Indole Synthesis 112 3.5 Fukuyama Indole Synthesis 125 3.6 Gassman Oxindole Synthesis 133 3.7 Larock Indole Synthesis 143 3.8 Matinet Dioxindole Reaction 167 3.9 Mori-Ban Indole Synthesis 175 3.10 Sandmeyer Isatin Synthesis 187 3.11 Sommelet-Hauser Rearrangement 197 3.12 Stolle Oxindole Synthesis 207 Chapter 4 Furans and Ox azoles 213 4.1 Nierenstein Reaction 214 4.2 Davidson Oxazole Synthesis 221 4.3 Fischer Oxazole Synthesis 225 4.4 Japp Oxazole Synthesis 233 4.5 Schhllkopf Oxazole Synthesis 242 Chapter 5 Other Five-Mem be red Heterocycles 259 5. L Bamberger Imidazole Cleavage 260 5.2 Dimroth Triazole Synthesis 269 5.3 Finnegan Tetrazole Synthesis 278 5.4 Hantzsch Thiazole Synthesis 299 5.5 Huisgen Tetrazole Rearrangement 309 5.6 Knorr Pyrazole Synthesis 317 5.7 Pechmann Pyrazole Synthesis 327 Part 3 Six-Membered Heterocycles 337 Chapter 6 Pyridincs 337 6.1 Baeyer Pyridine Synthesis 338 6.2 Katrizky Pyridine Synthesis 347 Chapter 7 Quinolines and Isoquinolines 351 7.1 Betti Reaction 352 7.2 Bemthsen Acridine Synthesis 360 7.3 Lehmstedt-Tanasescu Reaction 368 7.4 Niementowski Quinoline Synthesis 376 7.5 Povarov Reaction 385 Chapter 8 Six-Membered Heterocycles 401 8.1 Balaban-Nenitzescu-Praill Reaction 402 8.2 Borsche Cinnoline Synthesis 420 8.3 Gutknecht Pyrazine Synthesis 430 8.4 Niementowski Quinazoline Synthesis 440 8.5 Pechmann Coumarin Synthesis 454 8.6 Robin son-Schöpf Condensation 470 8.7 Simonis Chromone Cyclization 477 8.8 Wesseley--Moser Rearrangement 487 8.9 Widman-Stoermer Cinnoline Synthesis 493 8.10 Wichterle Reaction 497 Chapter 9 Miscellaneous Name Reactions 515 9.1 ANRORC Mechanism 516 9.2 Boulton-Katritzky Rearrangement 527 9.3 Chichibabin Animation Reaction 539 9.4 Dimroth Rearrangement 554 9.5 Hantzsch Synthesis 591 9.6 Ortolcva-King Reaction 645 Appendixes Appendix 1, Table of Contents for Volume 1: Name Reactions in Heterocyclic Chemistry 651 Appendix 2, Table of Contents for Volume 2: Name Reactions for Functional Group Transformations 655 Appendix 3, Table of Contents for Volume 3: Name Reactions for Hornolegations-I 657 Appendix 4, Table of Contents for Volume 4; Name Reactions for Hornohgations-II 659 Appendix 5, Table of Contents for Volume 5: Name Reactions for Ring Formations 661 Subject Index 663
Foreword. Preface. Contributing Authors. PART 1 THREE- AND FOUR-MEMBERED
HETEROCYCLES. Chapter 1 Aziridines and Epoxides. 1.1 Blum Aziridine
Synthesis. 1.2 Gabriel-Heine Aziridine Isomerization. 1.3 Shi Epoxidation.
PART 2 FIVE-MEMBERED HETEROCYCLES. Chapter 2 Pyrroles and Pyrrolidines. 2.1
Clauson-Kass Pyrrole Synthesis. 2.2 Houben-Hoech Acylation of Pyrroles. 2.3
Overman Pyrrolidine Synthesis. 2.4 Trofimov Synthesis of Pyrroles. Chapter
3 Indoles. 3.1 Bischler-Möhlau Indole Synthesis. 3.2 Borsche-Drechsel
Cyclization. 3.3 Buchwald-Hartwig Indole Synthesis. 3.4 Cadogan-Sundberg
Indole Synthesis. 3.5 Fukuyama Indole Synthesis. 3.6 Gassman Oxindole
Synthesis. 3.7 Larock Indole Synthesis. 3.8 Matinet Dioxindole Synthesis.
3.9 Mori-Ban Indole Synthesis. 3.10 Sandmeyer Isatin Synthesis. 3.11
Sommelet-Hauser Rearrangement. 3.12 Stollé Oxindole Synthesis. Chapter 4
Furans and Oxazoles. 4.1 Nierenstein Reaction. 4.2 Davidson Oxazole
Synthesis. 4.3 Fischer Oxazole Synthesis. 4.4 Japp Oxazole Synthesis. 4.5
Schöllkopf Oxazole Synthesis. Chapter 5 Other Five-Membered Heterocycles.
5.1 Bamberger Imidazole Cleavage. 5.2 Dimroth Triazole Synthesis. 5.3
Finnegan Tetrazole Synthesis. 5.4 Hantsch Thiazole Synthesis. 5.5 Huisgen
Tetrazole Rearrangement. 5.6 Knorr Pyrazole Synthesis. 5.7 Pechmann
Pyrazole Synthesis. PART 3 SIX-MEMBERED HETEROCYCLES. Chapter 6 Pyridines.
6.1 Baeyer Pyridine Synthesis. 6.2 Katrizky Reaction. Chapter 7 Quinolines
and Isoquinolines. 7.1 Betti reaction. 7.2 Bernthsen Acridine Synthesis.
7.3 Lehmstedt-Tanasescu Reaction. 7.4 Niementowski Quinoline Synthesis. 7.5
Povarov Reaction. Chapter 8 Six-Membered Heterocycles. 8.1
Balaban-Nenitzescu-Praill Reaction. 8.2 Borsche Cinnoline Synthesis. 8.3
Gutknecht Pyrazine Synthesis. 8.4 Niementowski Quinazoline Synthesis. 8.5
Pechmann Coumarin Synthesis. 8.6 Robinson-Schöpf Condensation. 8.7 Simonis
Chromone Cyclization. 8.8 Wesseley-Moser Rearrangement. 8.9 Widman-Stoermer
Cinnoline Synthesis. 8.10 Wichterle Reaction. Chapter 9 Miscellaneous Name
Reactions. 9.1 ANRORC Mechanism. 9.2 Boulton-Katritzky Rearrangement. 9.3
Chichibabin Amination Reaction. 9.4 Dimroth Rearrangement. 9.5 Hantzsch
Synthesis. 9.6 Ortoleva-King Reaction. Appendices. Appendix 1, Table of
Contents for Volume 1: Name Reactions in Heterocyclic Chemistry. Appendix
2, Table of Contents for Volume 2: Name Reactions for Functional Group
Transformations. Appendix 3, Table of Contents for Volume 3: Name Reactions
for Homologations-I. Appendix 4, Table of Contents for Volume 4: Name
Reactions for Homologations-II. Appendix 5, Table of Contents for Volume 5:
Name Reactions for Ring Formations.
HETEROCYCLES. Chapter 1 Aziridines and Epoxides. 1.1 Blum Aziridine
Synthesis. 1.2 Gabriel-Heine Aziridine Isomerization. 1.3 Shi Epoxidation.
PART 2 FIVE-MEMBERED HETEROCYCLES. Chapter 2 Pyrroles and Pyrrolidines. 2.1
Clauson-Kass Pyrrole Synthesis. 2.2 Houben-Hoech Acylation of Pyrroles. 2.3
Overman Pyrrolidine Synthesis. 2.4 Trofimov Synthesis of Pyrroles. Chapter
3 Indoles. 3.1 Bischler-Möhlau Indole Synthesis. 3.2 Borsche-Drechsel
Cyclization. 3.3 Buchwald-Hartwig Indole Synthesis. 3.4 Cadogan-Sundberg
Indole Synthesis. 3.5 Fukuyama Indole Synthesis. 3.6 Gassman Oxindole
Synthesis. 3.7 Larock Indole Synthesis. 3.8 Matinet Dioxindole Synthesis.
3.9 Mori-Ban Indole Synthesis. 3.10 Sandmeyer Isatin Synthesis. 3.11
Sommelet-Hauser Rearrangement. 3.12 Stollé Oxindole Synthesis. Chapter 4
Furans and Oxazoles. 4.1 Nierenstein Reaction. 4.2 Davidson Oxazole
Synthesis. 4.3 Fischer Oxazole Synthesis. 4.4 Japp Oxazole Synthesis. 4.5
Schöllkopf Oxazole Synthesis. Chapter 5 Other Five-Membered Heterocycles.
5.1 Bamberger Imidazole Cleavage. 5.2 Dimroth Triazole Synthesis. 5.3
Finnegan Tetrazole Synthesis. 5.4 Hantsch Thiazole Synthesis. 5.5 Huisgen
Tetrazole Rearrangement. 5.6 Knorr Pyrazole Synthesis. 5.7 Pechmann
Pyrazole Synthesis. PART 3 SIX-MEMBERED HETEROCYCLES. Chapter 6 Pyridines.
6.1 Baeyer Pyridine Synthesis. 6.2 Katrizky Reaction. Chapter 7 Quinolines
and Isoquinolines. 7.1 Betti reaction. 7.2 Bernthsen Acridine Synthesis.
7.3 Lehmstedt-Tanasescu Reaction. 7.4 Niementowski Quinoline Synthesis. 7.5
Povarov Reaction. Chapter 8 Six-Membered Heterocycles. 8.1
Balaban-Nenitzescu-Praill Reaction. 8.2 Borsche Cinnoline Synthesis. 8.3
Gutknecht Pyrazine Synthesis. 8.4 Niementowski Quinazoline Synthesis. 8.5
Pechmann Coumarin Synthesis. 8.6 Robinson-Schöpf Condensation. 8.7 Simonis
Chromone Cyclization. 8.8 Wesseley-Moser Rearrangement. 8.9 Widman-Stoermer
Cinnoline Synthesis. 8.10 Wichterle Reaction. Chapter 9 Miscellaneous Name
Reactions. 9.1 ANRORC Mechanism. 9.2 Boulton-Katritzky Rearrangement. 9.3
Chichibabin Amination Reaction. 9.4 Dimroth Rearrangement. 9.5 Hantzsch
Synthesis. 9.6 Ortoleva-King Reaction. Appendices. Appendix 1, Table of
Contents for Volume 1: Name Reactions in Heterocyclic Chemistry. Appendix
2, Table of Contents for Volume 2: Name Reactions for Functional Group
Transformations. Appendix 3, Table of Contents for Volume 3: Name Reactions
for Homologations-I. Appendix 4, Table of Contents for Volume 4: Name
Reactions for Homologations-II. Appendix 5, Table of Contents for Volume 5:
Name Reactions for Ring Formations.