Cumulenes in click reactions:
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
Chichester
Wiley
2009
|
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | Includes bibliographical references and index |
| Beschreibung: | X, 552 S. graph. Darst. |
| ISBN: | 9780470779323 |
Internformat
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Datensatz im Suchindex
| _version_ | 1804141152164642816 |
|---|---|
| adam_text | Titel: Cumulenes in click reactions
Autor: Ulrich, Henri
Jahr: 2009
Contents
Preface ix
Acknowledgements xi
1 General Introduction 1
References 12
2 1-Carbon Cumulenes 13
2.1 Sulfines, R2C=S=0 13
2.1.1 Introduction 13
2.1.2 Dimerization Reactions 14
2.1.3 Cycloaddition Reactions 15
References 23
2.2 Sulfenes, R2C=S(0)=0 25
2.2.1 Introduction 25
2.2.2 Dimerization Reactions 26
2.2.3 Cycloaddition Reactions 26
References 32
2.3 Other 1-Carbon Cumulenes 33
2.3.1 Thiocarbonyl 5-Imides 33
2.3.2 Thiocarbonyl 5-Sulfides 37
2.3.3 1 -Aza-2-azoniaalIene Salts 39
References 44
3 2-Carbon Cumulenes 45
3.1 Carbon Oxides, 0=C=0, :C=0 45
3.1.1 Introduction 45
3.1.2 Cycloaddition Reactions 47
3.1.3 Insertion Reactions
References
3.2.1 Introduction
3.2.3 Insertion Reactions
60
61
3.2 Carbon Sulfides, S=C=S. S=C=0 64
64
3.2.2 Cycloaddition Reactions 5
75
References
3.3 Carbon Nitrides 79
3.3.1 Isocyanates. RN=C=0 79
References
156
vi Contents
3.3.2 Isothiocyanates, RN=C=S 168
References 194
3.3.3 Carbodiimides, RN=C=NR 197
References 232
3.4 Center Carbon Phosphorallenes, P=C=P 236
3.4.1 Introduction 236
3.4.2 Dimerization Reactions 236
3.4.3 Cycloaddition Reactions 238
References 241
4 1,2-Dicarbon Cumulenes 243
4.1 Ketenes, R2C=C=0 243
4.1.1 Introduction 243
4.1.2 Dimerization Reactions 244
4.1.3 Trimerization Reactions 252
4.1.4 Cycloaddition Reactions 254
References 312
4.2 Thioketenes, R2C=C=S 321
4.2.1 Introduction 321
4.2.2 Dimerization Reactions 322
4.2.3 Cycloaddition Reactions 323
References 335
4.3 Ketenimines, R2C=C=NR 337
4.3.1 Introduction 337
4.3.2 Dimerization Reactions 337
4.3.3 Cycloaddition Reactions 339
References 363
4.4 l-Silaallenes,R2C=C=Si 366
4.4.1 Introduction 366
4.4.2 Dimerization Reactions 366
4.4.3 Cycloaddition Reactions 367
References 368
4.5 1-Phosphaallenes, R2C=C=P 368
4.5.1 Introduction 368
4.5.2 Dimerization Reactions 369
4.5.3 Cycloaddition Reactions 370
References 376
4.6 Other Metal Allenes 377
4.6.1 Introduction 377
4.6.2 Cycloaddition Reactions 378
References 389
5 13-Dicarbon Cumulenes 391
5.1 Thiocarbonyl S-ylides, R2C=S=CH2 391
5.2 2-Azaallenium Salts, R2C=N+=CR2 394
5.3 l-Oxa-3-azoniabutatriene Salts, R2C=N+=C=0 395
Contents vii
5.4 l-Thia-3-azabutatriene Salts, R2C=N+=C=S 396
5.5 Phosphorus Ylides 397
References 397
6 1,2,3-Tricarbon Cumulenes 399
6.1 Allenes, R2C=C=CR2 399
6.1.1 Introduction 399
6.1.2 Dimerization Reactions 402
6.1.3 Oligomerization Reactions 410
6.1.4 Cycloaddition Reactions 412
References 456
6.2 [3] Cumulenes, R2C=C=C=CR2 462
6.2.1 Introduction 462
6.2.2 Dimerization Reactions 462
6.2.3 Trimerization Reactions 464
6.2.4 Cycloaddition Reactions 465
References 468
6.3 [4] Cumulenes, R2C=C=C=C=CR2 469
6.3.1 Introduction 469
6.3.2 Dimerization Reactions 469
6.3.3 Cycloaddition Reactions 470
References 470
6.4 [5] Cumulenes, R2C=C=C=C=C=CR2 470
6.4.1 Introduction 470
6.4.2 Dimerization Reactions 471
6.4.3 Cycloaddition Reactions 472
References 473
7 Noncarbon Cumulenes 475
7.1 Azides, RN=N=N 475
7.1.1 Introduction 475
7.1.2 Oligomers 476
7.1.3 [34-2] Cycloaddition Reactions 477
References 492
7.1.4 Some Applications in Modifications of Biopolymers 495
Application References 499
7.2 Triazaallenium Salts, RN=N+=NR 501
7.2.1 Introduction 501
7.2.2 Cycloaddition Reactions 501
References 502
7.3 Sulfur Oxides 503
7.3.1 Introduction 503
7.3.2 Sulfur Dioxide, 0=S=0 504
7.3.3 Sulfur Trioxide, 0=S02 510
References 515
viii Contents
7.4 Sulfur Nitrides 517
7.4.1 Af-Sultinylamines, RN=S=0 and Af-Thiosulfinylamines, RN=S=S 517
7.4.2 Sulfurdiimines, RN=S=NR 526
7.4.3 Af-Sulfonylamines, RN=S02 and Hexavalent Sulfurdiimides 529
7.4.4 Dithionitronium Salts, S=N+=N 533
References 536
7.5 Cationic Boron Cumulenes, R2N=B=NR 538
7.5.1 Introduction 538
7.5.2 Cycloadditions 539
References 540
Index 541
|
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| spelling | Ulrich, Henri Verfasser aut Cumulenes in click reactions Henri Ulrich Chichester Wiley 2009 X, 552 S. graph. Darst. txt rdacontent n rdamedia nc rdacarrier Includes bibliographical references and index Alkenes Chemical reactions Kumulene (DE-588)4166000-6 gnd rswk-swf Organische Synthese (DE-588)4075695-6 gnd rswk-swf Heterokumulene (DE-588)4159740-0 gnd rswk-swf Click-Chemie (DE-588)7700321-4 gnd rswk-swf Kumulene (DE-588)4166000-6 s Organische Synthese (DE-588)4075695-6 s Click-Chemie (DE-588)7700321-4 s DE-604 Heterokumulene (DE-588)4159740-0 s HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=018980383&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Ulrich, Henri Cumulenes in click reactions Alkenes Chemical reactions Kumulene (DE-588)4166000-6 gnd Organische Synthese (DE-588)4075695-6 gnd Heterokumulene (DE-588)4159740-0 gnd Click-Chemie (DE-588)7700321-4 gnd |
| subject_GND | (DE-588)4166000-6 (DE-588)4075695-6 (DE-588)4159740-0 (DE-588)7700321-4 |
| title | Cumulenes in click reactions |
| title_auth | Cumulenes in click reactions |
| title_exact_search | Cumulenes in click reactions |
| title_full | Cumulenes in click reactions Henri Ulrich |
| title_fullStr | Cumulenes in click reactions Henri Ulrich |
| title_full_unstemmed | Cumulenes in click reactions Henri Ulrich |
| title_short | Cumulenes in click reactions |
| title_sort | cumulenes in click reactions |
| topic | Alkenes Chemical reactions Kumulene (DE-588)4166000-6 gnd Organische Synthese (DE-588)4075695-6 gnd Heterokumulene (DE-588)4159740-0 gnd Click-Chemie (DE-588)7700321-4 gnd |
| topic_facet | Alkenes Chemical reactions Kumulene Organische Synthese Heterokumulene Click-Chemie |
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