Book contents
- Frontmatter
- Contents
- Foreword
- Preface
- Abbreviations and Acronyms
- PART I
- 1 Arndt-Eistert Reaction
- 2 Baeyer-Villiger Oxidation
- 3 Baker-Venkatraman Rearrangement
- 4 Baker's yeast Enzymatic Synthesis
- 5 Bamford-Stevens Reaction
- 6 Barbier-Wieland Degradation
- 7 Barbier Reaction
- 8 Bart Reaction
- 9 Barton Decarboxylation
- 10 Barton-McCombie Reaction
- 11 Barton Reaction
- 12 Baylis-Hillman Reaction
- 13 Bechamp Reaction
- 14 Bechamp Reduction
- 15 Beckmann Rearrangement
- 16 Benzilic Acid Rearrangement
- 17 Benzoin Condensation
- 18 Birch Reduction
- 19 Blanc Chloromethylation Reaction
- 20 Bouveault-Blanc Reduction
- 21 Bouveault Aldehyde Synthesis
- 22 Bucherer Reaction
- 23 Cannizzaro Reaction
- 24 Chapman Rearrangement
- 25 Chugaev Reaction
- 26 Claisen Condensation
- 27 Claisen Rearrangement
- 28 Claisen Reaction
- 29 Claisen-Schmidt Condensation
- 30 Clemmensen Reduction
- 31 Cope Elimination
- 32 Cope Rearrangement
- 33 Corey-Bakshi-Shibata Reaction (CBS-Reaction)
- 34 Curtius Reaction
- 35 Dakin Reaction
- 36 Dakin-West Acylation Reaction
- 37 Darzens-Nenitzescu Synthesis
- 38 Delepine Reaction
- 39 Dieckmann Reaction
- 40 Diels-Alder Reaction
- 41 Duff Reaction
- 42 Elbs Reaction
- 43 Elbs Persulphate Oxidation
- 44 Emde Degradation
- 45 Ene Reaction
- 46 Etard Reaction
- 47 Favorskii Rearrangement
- 48 Friedel-Crafts Reaction
- 49 Fries Reaction
- 50 Gabriel Synthesis
- 51 Gattermann Reaction
- 52 Gattermann Aldehyde Synthesis
- 53 Gattermann-Koch Reaction
- 54 Gomberg-Bachmann-Hey Reaction
- 55 Griess Diazo Reaction
- 56 Grignard Reaction
- 57 Haloform Reaction
- 58 Hell-Volhard-Zelinsky Reaction
- 59 Hofmann Degradration
- 60 Hofmann Rearrangement
- 61 Hofmann Isonitrile Synthesis
- 62 Hofmann-Martius Rearrangement
- 63 Houben-Hoesch Synthesis
- 64 Hunsdiecker-Borodine Reaction
- 65 Hydroboration
- 66 Ivanov Reaction
- 67 Jacobsen Rearrangement
- 68 Japp-Klingemann Reaction
- 69 Kiliani-Fischer Synthesis
- 70 Knoevenagel Condensation
- 71 Koch Reaction
- 72 Kochi Reaction
- 73 Kolbe Electrolytic Synthesis
- 74 Kolbe-Schmitt Reaction
- 75 Leuckart-Wallach Reaction
- 76 Lossen Rearrangement
- 77 Malaprade Reaction
- 78 Mannich Reaction
- 79 McFadyen-Stevens Reduction
- 80 McLafferty Rearrangement
- 81 Meerwein-Ponndorf-Verley Reaction
- 82 Michael Reaction
- 83 Mitsunobu Reaction
- 84 Nazarov Cyclisation Reaction
- 85 Neber Rearrangement
- 86 Nef Reaction
- 87 Norrish Type I an II Reaction (Cleavage)
- 88 Oppenauer Oxidation
- 89 Orton Rearrangement
- 90 Passerini Reaction
- 91 Perkin Reaction
- 92 Pr'evost Reaction
- 93 Prins Reaction
- 94 Pschorr Synthesis
- 95 Reformatsky Reaction
- 96 Reimer-Tiemann Reaction
- 97 Robinson Annulation
- 98 Rosenmund Reaction
- 99 Sandmeyer Reaction
- 100 Sarett Oxidation
- 101 Schmidt Reaction
- 102 Scholl Reaction
- 103 Schotten-Baumann Reaction
- 104 Smiles Rearrangement
- 105 Sommelet Reaction
- 106 Stephen Reduction
- 107 Stevens Rearrangement
- 108 Stobbe Condensation
- 109 Stork Enamine Reaction
- 110 Suzuki Coupling
- 111 Ullmann Reaction
- 112 Vilsmeier-Haack Reaction
- 113 von Braun Reaction (vaun Braun Degradation)
- 114 Wagner-Meerwein Rearrangement
- 115 Willgerodt Reaction
- 116 Williamson Ether Synthesis
- 117 Wittig Reaction
- 118 Wohl-Ziegler Reaction
- 119 Wolff-Kishner Reduction
- 120 Wurtz Reaction
- PART II Heterocyclic Reactions
- Appendix I Some Popular Name Reactions
- Appendix II Select Bibliography
107 - Stevens Rearrangement
from PART I
Published online by Cambridge University Press: 05 February 2012
- Frontmatter
- Contents
- Foreword
- Preface
- Abbreviations and Acronyms
- PART I
- 1 Arndt-Eistert Reaction
- 2 Baeyer-Villiger Oxidation
- 3 Baker-Venkatraman Rearrangement
- 4 Baker's yeast Enzymatic Synthesis
- 5 Bamford-Stevens Reaction
- 6 Barbier-Wieland Degradation
- 7 Barbier Reaction
- 8 Bart Reaction
- 9 Barton Decarboxylation
- 10 Barton-McCombie Reaction
- 11 Barton Reaction
- 12 Baylis-Hillman Reaction
- 13 Bechamp Reaction
- 14 Bechamp Reduction
- 15 Beckmann Rearrangement
- 16 Benzilic Acid Rearrangement
- 17 Benzoin Condensation
- 18 Birch Reduction
- 19 Blanc Chloromethylation Reaction
- 20 Bouveault-Blanc Reduction
- 21 Bouveault Aldehyde Synthesis
- 22 Bucherer Reaction
- 23 Cannizzaro Reaction
- 24 Chapman Rearrangement
- 25 Chugaev Reaction
- 26 Claisen Condensation
- 27 Claisen Rearrangement
- 28 Claisen Reaction
- 29 Claisen-Schmidt Condensation
- 30 Clemmensen Reduction
- 31 Cope Elimination
- 32 Cope Rearrangement
- 33 Corey-Bakshi-Shibata Reaction (CBS-Reaction)
- 34 Curtius Reaction
- 35 Dakin Reaction
- 36 Dakin-West Acylation Reaction
- 37 Darzens-Nenitzescu Synthesis
- 38 Delepine Reaction
- 39 Dieckmann Reaction
- 40 Diels-Alder Reaction
- 41 Duff Reaction
- 42 Elbs Reaction
- 43 Elbs Persulphate Oxidation
- 44 Emde Degradation
- 45 Ene Reaction
- 46 Etard Reaction
- 47 Favorskii Rearrangement
- 48 Friedel-Crafts Reaction
- 49 Fries Reaction
- 50 Gabriel Synthesis
- 51 Gattermann Reaction
- 52 Gattermann Aldehyde Synthesis
- 53 Gattermann-Koch Reaction
- 54 Gomberg-Bachmann-Hey Reaction
- 55 Griess Diazo Reaction
- 56 Grignard Reaction
- 57 Haloform Reaction
- 58 Hell-Volhard-Zelinsky Reaction
- 59 Hofmann Degradration
- 60 Hofmann Rearrangement
- 61 Hofmann Isonitrile Synthesis
- 62 Hofmann-Martius Rearrangement
- 63 Houben-Hoesch Synthesis
- 64 Hunsdiecker-Borodine Reaction
- 65 Hydroboration
- 66 Ivanov Reaction
- 67 Jacobsen Rearrangement
- 68 Japp-Klingemann Reaction
- 69 Kiliani-Fischer Synthesis
- 70 Knoevenagel Condensation
- 71 Koch Reaction
- 72 Kochi Reaction
- 73 Kolbe Electrolytic Synthesis
- 74 Kolbe-Schmitt Reaction
- 75 Leuckart-Wallach Reaction
- 76 Lossen Rearrangement
- 77 Malaprade Reaction
- 78 Mannich Reaction
- 79 McFadyen-Stevens Reduction
- 80 McLafferty Rearrangement
- 81 Meerwein-Ponndorf-Verley Reaction
- 82 Michael Reaction
- 83 Mitsunobu Reaction
- 84 Nazarov Cyclisation Reaction
- 85 Neber Rearrangement
- 86 Nef Reaction
- 87 Norrish Type I an II Reaction (Cleavage)
- 88 Oppenauer Oxidation
- 89 Orton Rearrangement
- 90 Passerini Reaction
- 91 Perkin Reaction
- 92 Pr'evost Reaction
- 93 Prins Reaction
- 94 Pschorr Synthesis
- 95 Reformatsky Reaction
- 96 Reimer-Tiemann Reaction
- 97 Robinson Annulation
- 98 Rosenmund Reaction
- 99 Sandmeyer Reaction
- 100 Sarett Oxidation
- 101 Schmidt Reaction
- 102 Scholl Reaction
- 103 Schotten-Baumann Reaction
- 104 Smiles Rearrangement
- 105 Sommelet Reaction
- 106 Stephen Reduction
- 107 Stevens Rearrangement
- 108 Stobbe Condensation
- 109 Stork Enamine Reaction
- 110 Suzuki Coupling
- 111 Ullmann Reaction
- 112 Vilsmeier-Haack Reaction
- 113 von Braun Reaction (vaun Braun Degradation)
- 114 Wagner-Meerwein Rearrangement
- 115 Willgerodt Reaction
- 116 Williamson Ether Synthesis
- 117 Wittig Reaction
- 118 Wohl-Ziegler Reaction
- 119 Wolff-Kishner Reduction
- 120 Wurtz Reaction
- PART II Heterocyclic Reactions
- Appendix I Some Popular Name Reactions
- Appendix II Select Bibliography
Summary
- Type
- Chapter
- Information
- Name Reactions in Organic Synthesis , pp. 395 - 397Publisher: Foundation BooksPrint publication year: 2006