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Organic Reaction Mechanisms 2012, the 48th annual volume in this highly successful and unique series, surveys research on organic reaction mechanisms described in the available literature dated 2012. The following classes of organic reaction mechanisms are comprehensively reviewed:
An experienced team of authors compiled these reviews, ensuring the quality of selection and presentation.
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Seitenzahl: 1149
Veröffentlichungsjahr: 2015
Cover
Title Page
Copyright
Contributors
Preface
Chapter 1: Reactions of Aldehydes and Ketones and their Derivatives
Chapter 2: Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and their Derivatives
Intermolecular Catalysis and Reactions
Intramolecular Catalysis and Neighbouring Group Participation
Association-Prefaced Catalysis
Biologically Significant Reactions
Chapter 3: Oxidation and Reduction
Chapter 4: Carbenes and Nitrenes
Chapter 5: Aromatic Substitution
Chapter 6: Carbocations
Chapter 7: Nucleophilic Aliphatic Substitution
Chapter 8: Carbanions and Electrophilic Aliphatic Substitution
Chapter 9: Elimination Reactions
Chapter 10: Addition Reactions: Polar Addition
Chapter 11: Addition Reactions: Cycloaddition
Chapter 12: Molecular Rearrangements
Author Index
Subject Index
End User License Agreement
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Cover
Table of Contents
Preface
Begin Reading
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 14
Scheme 15
Scheme 16
Scheme 17
Scheme 18
Scheme 19
Scheme 20
Scheme 21
Scheme 22
Scheme 23
Scheme 24
Scheme 25
Scheme 26
Scheme 27
Scheme 28
Scheme 29
Scheme 30
Scheme 31
Scheme 32
Scheme 33
Scheme 34
Scheme 35
Scheme 36
Scheme 37
Scheme 38
Scheme 39
Scheme 40
Scheme 41
Scheme 42
Scheme 43
Scheme 44
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 14
Scheme 15
Scheme 16
Scheme 17
Scheme 18
Scheme 19
Scheme 20
Scheme 21
Scheme 22
Scheme 23
Scheme 24
Scheme 25
Scheme 26
Scheme 27
Scheme 28
Scheme 29
Scheme 30
Scheme 31
Scheme 32
Scheme 33
Scheme 34
Scheme 35
Scheme 36
Scheme 37
Scheme 38
Scheme 39
Scheme 40
Scheme 41
Scheme 42
Scheme 43
Scheme 44
Scheme 45
Scheme 46
Scheme 47
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 14
Scheme 15
Scheme 16
Scheme 17
Scheme 18
Scheme 19
Scheme 20
Scheme 21
Scheme 22
Scheme 23
Scheme 24
Scheme 25
Scheme 26
Scheme 27
Scheme 28
Scheme 29
Scheme 30
Scheme 31
Scheme 32
Scheme 33
Scheme 34
Scheme 35
Scheme 36
Scheme 37
Scheme 38
Scheme 39
Scheme 40
Scheme 41
Scheme 42
Scheme 43
Scheme 44
Scheme 45
Scheme 46
Scheme 47
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 14
Scheme 15
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 1
Scheme 2
Scheme 3
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 14
Scheme 15
Scheme 16
Scheme 17
Scheme 18
Scheme 19
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 14
Scheme 15
Scheme 16
Scheme 17
Scheme 18
Scheme 19
Scheme 20
Scheme 21
Scheme 22
Scheme 23
Scheme 24
Scheme 25
Scheme 26
Scheme 27
Scheme 28
Scheme 29
Scheme 30
Scheme 31
Scheme 32
Scheme 33
Scheme 34
Scheme 35
Scheme 36
Scheme 37
Scheme 38
Scheme 39
Scheme 40
Scheme 41
Scheme 42
Scheme 43
Scheme 44
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Scheme 6
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 14
Scheme 15
Scheme 16
Scheme 17
Scheme 18
Scheme 19
Scheme 20
Scheme 21
Scheme 22
Scheme 23
Scheme 24
Scheme 25
Scheme 26
Scheme 27
Scheme 28
Scheme 29
Scheme 30
Scheme 31
Scheme 32
Scheme 33
Scheme 34
Scheme 35
Scheme 36
Scheme 37
Scheme 38
Scheme 39
Scheme 40
Scheme 41
Scheme 42
Scheme 43
Scheme 44
Scheme 45
Scheme 46
Scheme 47
Scheme 48
Scheme 49
Scheme 50
Scheme 51
Scheme 52
Scheme 53
Scheme 54
Scheme 55
Scheme 56
Scheme 57
Scheme 58
Scheme 59
Scheme 60
Scheme 61
Scheme 62
Scheme 63
Scheme 64
Scheme 65
Scheme 66
Scheme 67
Scheme 68
Scheme 69
Scheme 70
Scheme 71
Scheme 72
Scheme 73
Scheme 74
Scheme 75
Scheme 76
Scheme 77
Scheme 78
Scheme 79
Scheme 80
Scheme 81
Scheme 82
Scheme 83
Scheme 84
Scheme 85
Scheme 86
Scheme 87
Scheme 88
Scheme 89
Scheme 90
Scheme 91
Scheme 92
Scheme 93
Scheme 94
Scheme 95
Scheme 96
Scheme 97
Scheme 98
Scheme 99
Scheme 100
Scheme 101
Scheme 102
Scheme 103
Scheme 104
Scheme 105
Scheme 106
Scheme 107
Scheme 108
Scheme 109
Scheme 110
Scheme 111
Scheme 112
Scheme 113
Scheme 114
Scheme 115
Scheme 116
Scheme 117
Scheme 118
Scheme 119
Scheme 120
Scheme 121
Scheme 122
Scheme 123
Scheme 124
Scheme 125
Scheme 126
Scheme 127
Scheme 128
Scheme 129
Scheme 130
Scheme 131
Scheme 132
Scheme 133
Scheme 134
Scheme 135
Scheme 136
Scheme 137
Scheme 138
Scheme 139
Scheme 140
Scheme 141
Scheme 142
Scheme 143
Scheme 144
Scheme 145
Scheme 146
Scheme 147
Scheme 148
Scheme 149
Scheme 150
Scheme 151
Scheme 152
Scheme 153
Scheme 154
Scheme 155
Scheme 156
Scheme 157
Scheme 158
Scheme 159
Scheme 160
Scheme 161
Scheme 162
Scheme 163
Scheme 164
Scheme 165
Scheme 166
Scheme 167
Scheme 168
Scheme 169
Scheme 170
Scheme 171
Scheme 172
Scheme 173
Scheme 174
Scheme 175
Scheme 176
Scheme 177
Scheme 178
Scheme 179
Scheme 180
Scheme 181
Scheme 182
Scheme 183
Scheme 184
Scheme 185
Scheme 186
Scheme 187
Scheme 188
Scheme 189
Scheme 190
Scheme 191
Scheme 192
Scheme 193
Edited by
A. C. Knipe
University of Ulster Northern Ireland
This edition first published 2015
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Library of Congress Catalog Card Number 66-23143
British Library Cataloguing in Publication Data
A catalogue record for this book is available from the British Library
Print ISBN: 978-1-118-36259-4
K. K. BANERJI
Faculty of Science, National Law University, Mandore, Jodhpur 342304, India
C. T. BEDFORD
Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK
M. L. BIRSA
Faculty of Chemistry, “Al. I. Cuza” University of Iasi, Bd. Carol I, 11, Iasi 700506, Romania
S. CHASSAING
Centre National de la Recherche Scientifique, Université de Toulouse, Toulouse, FranceCentre Pierre Potier, ITAV, Université de Toulouse, F-31106 Toulouse, FranceINSA, F-31400 Toulouse, France
J. M. COXON
Department of Chemistry, University of Canterbury, Christchurch, New Zealand
M. R. CRAMPTON
Department of Chemistry, University of Durham, South Road, Durham, DH1 3LE, UK
N. DENNIS
3 Camphor Laurel Court, Stretton, Brisbane, Queensland 4116, Australia
E. GRAS
Laboratoire de Chimie de Coordination, Centre National de la Recherche Scientifique, Toulouse, France
A. C. KNIPE
Faculty of Life and Health Sciences, University of Ulster, Coleraine, Northern Ireland
P. KOČOVSKÝ
Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, Stockholm SE 10691, SwedenDepartment of Organic Chemistry, Charles University, 12843 Prague 2, Czech Republic
R. A. McCLELLAND
Department of Chemistry, University of Toronto, Toronto, 80 St George Street, Toronto, Ontario M5S 1A1, Canada
K. C. WESTAWAY
Department of Chemistry and Biochemistry, Laurentian University, Sudbury, Ontario P3E 2C6, Canada
The present volume, the 48th in the series, surveys research on organic reaction mechanisms described in the available literature dated 2012. In order to limit the size of the volume, it is necessary to exclude or restrict overlap with other publications which review specialist areas (e.g., photochemical reactions, biosynthesis, enzymology, electrochemistry, organometallic chemistry, surface chemistry, and heterogeneous catalysis). In order to minimize duplication, while ensuring a comprehensive coverage, the editor conducts a survey of all relevant literature and allocates publications to appropriate chapters. While a particular reference may be allocated to more than one chapter, it is assumed that readers will be aware of the alternative chapters to which a borderline topic of interest may have been preferentially assigned.
In view of the considerable interest in application of stereoselective reactions to organic synthesis, we now provide indication, in the margin, of reactions which occur with significant diastereomeric or enantiomeric excess (de or ee).
We are pleased to have retained for ORM 2012 our current team of experienced authors who have contributed to ORM volumes for periods of 7 to 34 years.
However, it is unfortunate that intervention of the editor to avoid an anticipated delay between title year and publication date for this volume was thwarted by unusually late arrival of a particularly long chapter. Nonetheless, we hope soon to regain our optimum production schedule.
I wish to thank the staff of John Wiley & Sons and our expert contributors for their efforts to ensure that the review standards of this series are sustained, particularly during a period of substantial reorganisation of production procedures.
A. C. K.
A.C. Knipe
Faculty of Life and Health Sciences, University of Ulster, Coleraine, Northern Ireland
Formation and Reactions of Acetals and Related Species
Reactions of Glucosides and Nucleosides
Reactions of Ketenes and Ketenimines
Formation and Reactions of Nitrogen Derivatives
Imines: Synthesis, Tautomerism, and Catalysis
The Mannich and Nitro-Mannich reactions
Addition of organometallics
Other alkenylations, allylations, and arylations of imines
Oxidation and reduction of imines
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