Name Reactions in Organic Chemistry
eBook - PDF

Name Reactions in Organic Chemistry

  1. 288 pages
  2. English
  3. PDF
  4. Available on iOS & Android
eBook - PDF

Name Reactions in Organic Chemistry

About this book

Name Reactions in Organic Chemistry, 2nd Edition, incorporates new, pertinent material and brings up to date the name reactions described in the first edition. Along with this revision, several additional name reactions have been included. As with the first edition, the selections were based on general interest, recurrence in the literature, and the contributions of the ""name chemist"" to the historical development of organic chemistry. Although the writer does not pretend to be an historian of chemistry, it seemed desirable to include, along with the reactions, pertinent information regarding the chemist's background, his training, his contemporaries, and his contributions. This book contains 103 name reactions, arranged alphabetically. The general plan was to present a description of each reaction, its scope, applicability, and limitations, and to bring it up to date in regard to any new developments.

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Yes, you can access Name Reactions in Organic Chemistry by Alexander R. Surrey in PDF and/or ePUB format, as well as other popular books in Physical Sciences & Chemistry. We have over one million books available in our catalogue for you to explore.

Information

Year
2013
Print ISBN
9781483232270
eBook ISBN
9781483258683
Edition
2
Subtopic
Chemistry

Table of contents

  1. Front Cover
  2. Name Reactions in Organic Chemistry
  3. Copyright Page
  4. Table of Contents
  5. Preface to Second Edition
  6. Preface to First Edition
  7. Chapter 1. Arndt-Eistert Synthesis
  8. Chapter 2. Baeyer-Villiger Oxidation
  9. Chapter 3. Barbier-Wieland Degradation
  10. Chapter 4. Bart Reaction
  11. Chapter 5. Bechamp Reduction
  12. Chapter 6. Beckmann Rearrangement
  13. Chapter 7. Birch Reduction
  14. Chapter 8. Bischler-Napieralski Reaction
  15. Chapter 9. Blanc Chloromethylation Reaction
  16. Chapter 10. Bouveault-Blanc1 Reduction
  17. Chapter 11. Bouveault Aldehyde Synthesis
  18. Chapter 12. Von Braun Reaction
  19. Chapter 13. Von Braun Degradation
  20. Chapter 14. Bucherer Reaction
  21. Chapter 15. Bucherer Hydantoin Synthesis
  22. Chapter 16. Camps Reaction
  23. Chapter 17. Cannizzaro Reaction
  24. Chapter 18. Chugaev Reaction
  25. Chapter 19. Claisen Condensation
  26. Chapter 20. Claisen Rearrangement
  27. Chapter 21. Claisen-Schmidt Condensation
  28. Chapter 22. Clemmensen Reduction
  29. Chapter 23. Combes Quinoline Synthesis
  30. Chapter 24. Conrad-Limpach Synthesis
  31. Chapter 25. Curtius Reaction
  32. Chapter 26. Dakin Reaction
  33. Chapter 27. Dakin-West Reaction
  34. Chapter 28. Darzens Glycidic Ester Condensation
  35. Chapter 29. Darzens Synthesis of Unsaturated Ketones
  36. Chapter 30. Delepine Reaction
  37. Chapter 31. Dieckmcmn Reaction
  38. Chapter 32. Diels-Alder Reaction
  39. Chapter 33. Doebner Synthesis
  40. Chapter 34. Doebner-Miller Synthesis
  41. Chapter 35. Duff Reaction
  42. Chapter 36. Elbs Reaction
  43. Chapter 37. Elbs Persulfate Oxidation
  44. Chapter 38. Emde Degradation
  45. Chapter 39. Erlenmeyer-Plochl Azlactone Synthesis
  46. Chapter 40. Faworskii Rearrangement
  47. Chapter 41. Fischer Indole Synthesis
  48. Chapter 42. Friedel-Crafts Reaction
  49. Chapter 43. Friedldnder Synthesis
  50. Chapter 44. Fries Reaction
  51. Chapter 45. Gabriel Synthesis
  52. Chapter 46. Gattermann Aldehyde Synthesis
  53. Chapter 47. Gattermann Reaction
  54. Chapter 48. Gattermann-Koch Reaction
  55. Chapter 49. Gomberg-Bachmann-Hey Reaction
  56. Chapter 50. Gould-Jacobs Reaction
  57. Chapter 51. Graebe-Ullmann Synthesis
  58. Chapter 52. Grignard Reaction
  59. Chapter 53. Hantzsch Pyridine Synthesis
  60. Chapter 54. Hell-Volhard-Zelinsky Reaction
  61. Chapter 55. Hoesch Synthesis
  62. Chapter 56. Hofmann Reaction
  63. Chapter 57. Hofmann Degradation
  64. Chapter 58. Hunsdiecker Reaction
  65. Chapter 59. Ivanov Reaction
  66. Chapter 60. Jacobsen Reaction
  67. Chapter 61. Knoevenagel Reaction
  68. Chapter 62. Knorr Pyrrole Synthesis -
  69. Chapter 63. Kolbe-Schmitt Reaction
  70. Chapter 64. Kolbe's Electrochemical Reaction
  71. Chapter 65. Leuckart Reaction
  72. Chapter 66. Lossen Rearrangement
  73. Chapter 67. McFadyen-Stevens Reduction
  74. Chapter 68. Mannich Reaction
  75. Chapter 69. Meerwein Condensation
  76. Chapter 70. Meerwein-Ponndorf-Verley Reduction
  77. Chapter 71. Michael Reaction
  78. Chapter 72. Nef Reaction
  79. Chapter 73. Oppenauer Oxidation
  80. Chapter 74. Passerini Reaction
  81. Chapter 75. Pechmann Condensation
  82. Chapter 76. Perkin Reaction
  83. Chapter 77. Pfitzinger Reaction
  84. Chapter 78. Pictet-Spengler Reaction
  85. Chapter 79. Pomeranz-Fritsch Reaction
  86. Chapter 80. Prins Reaction
  87. Chapter 81. Pschorr Synthesis
  88. Chapter 82. Reformatsky Reaction
  89. Chapter 83. Reimer-Tiemann Reaction
  90. Chapter 84. Reissert Reaction
  91. Chapter 85. Rosenmund Reduction
  92. Chapter 86. Sandmeyer Reaction
  93. Chapter 87. Schiemann Reaction
  94. Chapter 88. Schmidt Reaction
  95. Chapter 89. Skraup Reaction
  96. Chapter 90. Sommelet Reaction
  97. Chapter 91. Stephen Reaction
  98. Chapter 92. Stevens Rearrangement
  99. Chapter 93. Stobbe Condensation
  100. Chapter 94. Stork Reaction
  101. Chapter 95. Ullmann Reaction
  102. Chapter 96. Ullmann Condensation
  103. Chapter 97. Wallach Reaction
  104. Chapter 98. Willgerodt Reaction
  105. Chapter 99. Williamson Synthesis
  106. Chapter 100. Wittig Reaction
  107. Chapter 101. Wohl-Ziegler Reaction
  108. Chapter 102. Wolff-Kishner Reduction
  109. Chapter 103. Wurtz Reaction
  110. Subject Index