Palladium in Heterocyclic Chemistry -

Palladium in Heterocyclic Chemistry (eBook)

A Guide for the Synthetic Chemist
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2006 | 2. Auflage
658 Seiten
Elsevier Science (Verlag)
978-0-08-046584-5 (ISBN)
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199,27 inkl. MwSt
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Palladium chemistry, despite its immaturity, has rapidly become an indispensable tool for synthetic organic chemists. Heterocycles are of paramount importance in the pharmaceutical industry and palladium chemistry is one of the most novel and efficient ways of making heterocycles. Today, palladium-catalyzed coupling is the method of choice for the synthesis of a wide range of biaryls and heterobiaryls. The number of applications of palladium chemistry to the syntheses of heterocycles has grown exponentially.
These developments highlight the need for a monograph dedicated solely to the palladium chemistry in heterocycles and this book provides a comprehensive explanation of the subject. The principal aim of the book is to highlight important palladium-mediated reactions of heterocycles with emphasis on the unique characteristics of individual heterocycles.
1. Palladium chemistry of heterocycles has its idiosyncrasies stemming from their different structural properties from the corresponding carbocyclic aryl compounds. Even activated chloroheterocycles are sufficiently reactive to undergo Pd-catalyzed reactions. As a consequence of &agr and &bgr activation of heteroaryl halides, Pd-catalyzed chemistry may take place regioselectively at the activated positions, a phenomenon rarely seen in carbocyclic aryl halides. In addition, another salient peculiarity in palladium chemistry of heterocycles is the so-called heteroaryl Heck reaction. For instance, while intermolecular palladium-catalyzed arylations of carbocyclic arenes are rare, palladium-catalyzed arylations of azoles and many other heterocycles readily take place. Therefore, the principal aim of this book is to highlight important palladium-mediated reactions of heterocycles with emphasis on the unique characteristics of individual heterocycles.
2. A myriad of heterocycles are biologically active and therefore of paramount importance to medicinal and agricultural chemists. Many heterocycle-containing natural products (they are highlighted in boxes throughout the text) have elicited great interest from both academic and industrial research groups. Recognizing the similarities between the palladium chemistry of arenes and heteroarenes, a critical survey of the accomplishments in heterocyclic chemistry will keep readers abreast of such a fast-growing field. We also hope this book will spur more interest and inspire ideas in such an extremely useful area.
This book comprises a compilation of important preparations of heteroaryl halides, boranes and stannanes for each heterocycle. The large body of data regarding palladium-mediated polymerization of heterocycles in material chemistry is not focused here, neither is coordination chemistry involving palladium and heterocycles.
Many heterocycle-containing natural products (highlighted throughout the text) have elicited great interest from both academic and industrial research groups. Recognizing the similarities between the palladium chemistry of arenes and heteroarenes, a critical survey of the accomplishments in heterocyclic chemistry keeps readers abreast of this fast-growing field. It is also hoped that this book will stimulate more interest and inspire new ideas in this exciting area.

- Contains the most up-to-date developments in this fast-moving field
- Includes 3 new chapters
- Incorporates material from selected well-respected authors on heterocyclic chemistry
Palladium chemistry, despite its immaturity, has rapidly become an indispensable tool for synthetic organic chemists. Heterocycles are of paramount importance in the pharmaceutical industry and palladium chemistry is one of the most novel and efficient ways of making heterocycles. Today, palladium-catalyzed coupling is the method of choice for the synthesis of a wide range of biaryls and heterobiaryls. The number of applications of palladium chemistry to the syntheses of heterocycles has grown exponentially. These developments highlight the need for a monograph dedicated solely to the palladium chemistry in heterocycles and this book provides a comprehensive explanation of the subject. The principal aim of the book is to highlight important palladium-mediated reactions of heterocycles with emphasis on the unique characteristics of individual heterocycles. 1. Palladium chemistry of heterocycles has its "e;idiosyncrasies stemming from their different structural properties from the corresponding carbocyclic aryl compounds. Even activated chloroheterocycles are sufficiently reactive to undergo Pd-catalyzed reactions. As a consequence of &agr and &bgr activation of heteroaryl halides, Pd-catalyzed chemistry may take place regioselectively at the activated positions, a phenomenon rarely seen in carbocyclic aryl halides. In addition, another salient peculiarity in palladium chemistry of heterocycles is the so-called "e;heteroaryl Heck reaction"e;. For instance, while intermolecular palladium-catalyzed arylations of carbocyclic arenes are rare, palladium-catalyzed arylations of azoles and many other heterocycles readily take place. Therefore, the principal aim of this book is to highlight important palladium-mediated reactions of heterocycles with emphasis on the unique characteristics of individual heterocycles. 2. A myriad of heterocycles are biologically active and therefore of paramount importance to medicinal and agricultural chemists. Many heterocycle-containing natural products (they are highlighted in boxes throughout the text) have elicited great interest from both academic and industrial research groups. Recognizing the similarities between the palladium chemistry of arenes and heteroarenes, a critical survey of the accomplishments in heterocyclic chemistry will keep readers abreast of such a fast-growing field. We also hope this book will spur more interest and inspire ideas in such an extremely useful area. This book comprises a compilation of important preparations of heteroaryl halides, boranes and stannanes for each heterocycle. The large body of data regarding palladium-mediated polymerization of heterocycles in material chemistry is not focused here; neither is coordination chemistry involving palladium and heterocycles. Many heterocycle-containing natural products (highlighted throughout the text) have elicited great interest from both academic and industrial research groups. Recognizing the similarities between the palladium chemistry of arenes and heteroarenes, a critical survey of the accomplishments in heterocyclic chemistry keeps readers abreast of this fast-growing field. It is also hoped that this book will stimulate more interest and inspire new ideas in this exciting area. - Contains the most up-to-date developments in this fast-moving field- Includes 3 new chapters- Incorporates material from selected well-respected authors on heterocyclic chemistry

Front cover 1
Contents 12
Preface to the second edition 8
Preface to the first edition 10
Abbreviations 20
Chapter 1 An introduction to palladium catalysis 22
1.1 Oxidative coupling/cyclization 24
1.2 Cross-coupling reactions with organometallic reagents 26
1.3 The Sonogashira reaction 35
1.4 The Heck, intramolecular Heck, and heteroaryl Heck reactions 36
1.5 Carbonylation reactions 40
1.6 The Pd-catalyzed C-P bond formation 41
1.7 Palladium-catalyzed C-N bond and C-O bond-forming reactions 42
1.8 The Tsuji-Trost reaction 46
1.9 The Wacker-type reactions 47
1.10 Mori-Ban, Hegedus, and Larock indole syntheses 48
1.11 References 50
Chapter 2 Pyrroles 58
2.1 Synthesis of pyrrolyl halides 59
2.2 Oxidative coupling/cyclization 62
2.3 Coupling reactions with organometallic reagents 67
2.4 Sonogashira reaction 80
2.5 Heck and intramolecular Heck reactions 82
2.6 Carbonylation 87
2.7 C-N bond formation reactions 88
2.8 Miscellaneous 93
2.9 References 95
Chapter 3 Indoles 102
3.1 Synthesis of indolyl halides 104
3.2 Oxidative coupling/cyclization 111
3.3 Coupling reactions with organometallic reagents 117
3.4 The Sonogashira coupling 145
3.5 Heck couplings 149
3.6 Carbonylation 171
3.7 C-N bond formation reactions 176
3.8 Miscellaneous 186
3.9 References 189
Chapter 4 Pyridines 210
4.1 Synthesis of halopyridines 213
4.2 Coupling reactions with organometallic reagents 221
4.3 Sonogashira reaction 246
4.4 Heck and intramolecular Heck reactions 252
4.5 Buchwald-Hartwig aminations(C-N bond formation) 257
4.6 Direct C-C bond formation 261
4.7 Summary 263
4.8 References 264
Chapter 5 Thiophenes and benzo[b]thiophenes 272
5.1 Preparation of halothiophenes and halobenzothiophenes 273
5.2 Oxidative and reductive coupling reactions 277
5.3 Cross-coupling with organometallic reagents 277
5.4 Sonogashira reaction 305
5.5 Heck and intramolecular Heck reactions 308
5.6 Carbonylation reactions 311
5.7 Buchwald-Hartwig aminations 312
5.8 Miscellaneous 315
5.9 References 316
Chapter 6 Furans and benzo[b]furans 324
6.1 Synthesis of halofurans and halobenzo[b]furans 324
6.2 Oxidative coupling/cyclization 327
6.3 Coupling reactions with organometallic reagents 329
6.4 Sonogashira reaction 343
6.5 Heck, intramolecular Heck, and heteroaryl Heck reactions 345
6.6 Heteroannulation 349
6.7 Carbonylation and C-N and C-O bond formation 357
6.8 References 358
Chapter 7 Thiazoles and benzothiazoles 366
7.1 Synthesis of halothiazoles 366
7.2 Coupling reactions with organometallic reagents 368
7.3 Sonogashira reaction 384
7.4 Heck and heteroaryl Heck reactions 388
7.5 Carbonylation 391
7.6 C-N bond formation 392
7.7 Site selective coupling reactions 392
7.8 References 395
Chapter 8 Oxazoles and benzoxazoles 400
8.1 Introduction 400
8.2 Synthesis of halooxazoles and halobenzoxazoles 404
8.3 Coupling reactions with organometallic reagents 406
8.4 Heck and heteroaryl Heck reactions 419
8.5 Carbonylation 421
8.6 Palladium-catalyzed amination 423
8.7 Carbopalladation of nitriles 423
8.8 Quaterfuran and Quinquifuran 424
8.9 Summary 425
8.10 References 425
Chapter 9 Imidazoles 428
9.1 Synthesis of haloimidazoles 428
9.2 Homocoupling reaction 431
9.3 Coupling reactions with organometallic reagents 432
9.4 Sonogashira reaction 443
9.5 Heck and heteroaryl Heck reactions 445
9.6 Tsuji-Trost reaction 449
9.7 Phosphonylation 450
9.8 References 451
Chapter 10 Pyrazines and quinoxalines 456
10.1 Pyrazines 456
10.2 Coupling reactions with organometallic reagents 458
10.3 Palladium-catalyzed amination 476
10.4 Heck reaction 477
10.5 Carbonylation reactions 479
10.6 Cyanation of pyrazines 481
10.7 Deoxygenation of heteroamine-N-oxide 481
10.8 Quinoxalines 482
10.9 References 490
Chapter 11 Pyrimidines 496
11.1 Synthesis of pyrimidinyl halides and triflates 497
11.2 Coupling reactions with organometallic reagents 499
11.3 Sonogashira reaction 517
11.4 Heck reaction 523
11.5 The carbonylation reaction 525
11.6 Heteroannulation 526
11.7 References 527
Chapter 12 Quinolines 532
12.1 Synthesis of quinoline electrophiles 533
12.2 Synthesis of quinoline nucleophiles 538
12.3 Cross-coupling reactions with organometallic reagents 540
12.4 Sonogashira reaction 549
12.5 Heck reaction 551
12.6 Miscellaneous reactions mediated by palladium 554
12.7 References 558
Chapter 13 Pyridazines 562
13.1 Synthesis of (pseudo)halopyridazines and (pseudo)halopyridazin-3(2H)-ones 564
13.2 Coupling reactions with organometallic reagents 571
13.3 Sonogashira reaction 587
13.4 Heck and intramolecular Heck reactions 595
13.5 Carbonylation reactions 598
13.6 C-N bond formation 600
13.7 References 603
Chapter 14 Industrial scale palladium chemistry 608
14.1 Introduction 608
14.2 Pharmaceutical products 609
14.3 Cosmaceuticals 620
14.4 Agrochemical products 620
14.5 Material sciences 622
14.6 Polymer chemistry 624
14.7 New catalyst developments in fine chemical synthesis 628
14.8 Amination 633
14.9 Carbonylation 633
14.10 Amidocarbonylation 634
14.11 References 634
Index 642

Erscheint lt. Verlag 20.10.2006
Sprache englisch
Themenwelt Naturwissenschaften Chemie Anorganische Chemie
Naturwissenschaften Chemie Organische Chemie
Technik
ISBN-10 0-08-046584-6 / 0080465846
ISBN-13 978-0-08-046584-5 / 9780080465845
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