Jie Jack Li
Name Heterocyclic 2
Jie Jack Li
Name Heterocyclic 2
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Co-authored by Nobel Laureatte, E.J. Corey, this book builds on the first volume on this topic by presenting a comprehensive treatise on name reactions in heterocyclic chemistry. Primary topics include updates to the first volume on the new and/or expanded reactions in three and four-membered heterocycles, five-membered heterocycles, six-membered heterocycles. Each section includes a description of the reaction, the historical perspective, a mechanism for the reaction, variations and improvements on the reaction, synthetic utilities of the reaction, experimental details, and references to the current primary literature.…mehr
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Co-authored by Nobel Laureatte, E.J. Corey, this book builds on the first volume on this topic by presenting a comprehensive treatise on name reactions in heterocyclic chemistry. Primary topics include updates to the first volume on the new and/or expanded reactions in three and four-membered heterocycles, five-membered heterocycles, six-membered heterocycles. Each section includes a description of the reaction, the historical perspective, a mechanism for the reaction, variations and improvements on the reaction, synthetic utilities of the reaction, experimental details, and references to the current primary literature.
Produktdetails
- Produktdetails
- Verlag: John Wiley & Sons / Wiley
- Seitenzahl: 704
- Erscheinungstermin: 13. September 2011
- Englisch
- Abmessung: 241mm x 196mm x 42mm
- Gewicht: 1492g
- ISBN-13: 9780470085080
- ISBN-10: 0470085088
- Artikelnr.: 33256009
- Verlag: John Wiley & Sons / Wiley
- Seitenzahl: 704
- Erscheinungstermin: 13. September 2011
- Englisch
- Abmessung: 241mm x 196mm x 42mm
- Gewicht: 1492g
- ISBN-13: 9780470085080
- ISBN-10: 0470085088
- Artikelnr.: 33256009
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. 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. 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.