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Preface | ||
1 | Introduction | 1 |
2 | Aldol Condensation | 3 |
2.1 | Michael - Aldol Tandems | 4 |
2.2 | Claisen - Aldol and Multiple Aldol Condensations | 18 |
2.3 | Retro-Aldol - Aldol Tandems | 22 |
2.4 | Mannich - Aldol Tandems | 28 |
2.5 | Rearrangement - Aldol Tandems | 29 |
2.6 | Aldol-Type Reactions in Tandem with Other Processes | 31 |
3 | Michael Reactions | 33 |
3.1 | Michael Reactions Initiated by Other Reactions | 34 |
3.2 | Double Michael Reactions | 44 |
3.3 | Reflexive Michael Reactions | 50 |
4 | Tandem Vicinal Difunctionalization of Alkenes and Alkynes | 57 |
4.1 | Michael Reaction/Electrophilation | 57 |
4.2 | vic-Difunctionalization of Temporarily Activated Alkenes | 68 |
4.3 | Pauson - Khand Cyclization and Dotz Reaction | 70 |
4.4 | Intramolecular Metallo - Ene Reactions and Related CC Bond Formation Processes | 76 |
4.5 | Cationic Polyene Cyclizations | 82 |
4.6 | Miscellaneous vic-Dialkylations | 86 |
5 | Dieckmann and Claisen Cyclizations | 88 |
5.1 | Michael - Dieckmann and Michael - Claisen Reaction Tandems | 89 |
5.2 | Alkylation - Dieckmann and Related Tandem Reactions | 94 |
5.3 | Tandem Reactions Terminated by Claisen Condensation | 97 |
6 | Mannich Reaction | 100 |
6.1 | Schiff Condensation - Mannich Cyclization | 100 |
6.2 | Manifold Mannich Reactions | 106 |
6.3 | Alkylation or Acylation - Mannich Cyclization | 109 |
6.4 | Retro - Mannich Fragmentation - Mannich Cyclization | 117 |
6.5 | Mannich Cyclization Following Oxidation or Reduction | 122 |
6.6 | Cationic Aza-Cope Rearrangement - Mannich Cyclization and Others | 124 |
7 | Diels - Alder Reactions | 131 |
7.1 | Elimination/Diels - Alder Reaction Tandems | 131 |
7.2 | Retro-Diels - Alder/Diels - Alder Reactions | 144 |
7.3 | Electrocyclic/Diels - Alder Reactions | 150 |
7.4 | Diels - Alder Reactions Preceded by Other Pericyclic Reactions | 163 |
7.5 | Acylation/Diels - Alder Reaction Tandems | 176 |
7.6 | Oxidation or Reduction Initiated Diels - Alder Reactions | 178 |
7.7 | Intramolecularization | 182 |
7.8 | Assorted Triggers for the Diels - Alder Reaction | 188 |
8 | Other Cycloadditions | 202 |
8.1 | [2 + 2]-Cycloadditions | 202 |
8.2 | [2 + 2 + 2]-Cycloadditions | 205 |
8.3 | Formation of Five-Membered Rings by Concerted Cycloadditions | 209 |
8.4 | Higher-Order Cycloadditions | 215 |
8.5 | 1,3-Dipolar Cycloadditions | 221 |
9 | Retro-Diels - Alder and Cheletropic Reactions | 231 |
9.1 | Diels - Alder/Retro-Diels - Alder Reaction Tandems | 231 |
9.2 | Retro-Diels - Alder Reactions Following Other Processes | 250 |
9.3 | Some Other Cheletropic Reactions | 257 |
10 | Electrocyclic Reactions | 259 |
10.1 | Electrocyclic Reaction Cascades | 259 |
10.2 | Cycloaddition or Cycloreversion/Electrocyclic Reaction Tandems | 269 |
10.3 | Rearrangement - Electrocyclic Reaction Tandems | 275 |
10.4 | Electrocyclic Reactions Induced by Enolization, Elimination, Condensation, or Other Processes | 281 |
11 | Ene, Retro-Ene, and Some Other Thermal Reactions | 297 |
11.1 | Ene Reactions | 297 |
11.2 | Retro-Ene Reactions | 303 |
11.3 | Vinylcyclopropane-to-Cyclopentene Rearrangements | 306 |
12 | Sigmatropic Rearrangements | 308 |
12.1 | [1, n]-Sigmatropic Rearrangements | 308 |
12.2 | [3.3]-Sigmatropic Rearrangements | 320 |
13 | Rearrangements and Fragmentations | 361 |
13.1 | Rearrangements | 361 |
13.2 | Fragmentation Reactions | 377 |
14 | Free Radical Reactions | 398 |
14.1 | Vicinal CC Bond Formations | 399 |
14.2 | 1,3-Diyl Cycloadditions | 408 |
14.3 | Addition - Fragmentation Tandems | 409 |
14.4 | Reactions of Carbinyl Radicals Adjacent to a Small Ring | 412 |
14.5 | Miscellaneous Radical Reaction Tandems | 413 |
15 | Miscellaneous Tandem Reactions | 416 |
15.1 | Wittig and Related Reactions | 416 |
15.2 | Electrophilations | 426 |
15.3 | Eliminations and Ring Openings | 442 |
15.4 | Stitching of Alkenes and Alkynes | 445 |
15.5 | Tandem Reactions Involving Oxidoreductions | 447 |
References | 449 | |
Index | 493 |
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Add Tandem Organic Reactions, The importance of tandem reactions is evident—besides their pragmatic value, they have an aesthetic appeal. The author presents a survey of these reactions that will rivet the attention of numerous chemists to their merits and utility as well as stimulate, Tandem Organic Reactions to the inventory that you are selling on WonderClubX
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Add Tandem Organic Reactions, The importance of tandem reactions is evident—besides their pragmatic value, they have an aesthetic appeal. The author presents a survey of these reactions that will rivet the attention of numerous chemists to their merits and utility as well as stimulate, Tandem Organic Reactions to your collection on WonderClub |