Name Reactions A collection of detailed mechanisms and synthetic applications 6th Edition by Li Jie Jack ISBN 9783030508647 3030508641

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ISBN 10:   3030508641

ISBN 13: 9783030508647

Author: Li Jie Jack

 In this sixth edition of Jack Jie Li’s seminal “Name Reactions”, the author has added three or more synthetic applications of name reactions to reflect the recent advances in organic chemistry. As in previous editions, each reaction is delineated by its detailed step-by-step, electron-pushing mechanism and supplemented with the original and the latest references, especially from review articles. This book is not only an indispensable resource for advanced undergraduate and graduate students for learning and preparing exams, but is also a good reference book for all organic chemists in both industry and academia.  
Unlike other books on name reactions in organic chemistry, Name Reactions, A Collection of Detailed Reaction Mechanisms and Synthetic Applications focuses on the reaction mechanisms. It covers over 300 classical as well as contemporary name reactions.

Table of contents: 

1. Alder Ene Reaction

2. Aldol Condensation

3. Arndt–Eistert Homologation

4. Baeyer–Villiger Oxidation

5. Baker–Venkataraman Rearrangement

6. Bamford–Stevens Reaction

7. Barbier Reaction

8. Barton–McCombie Deoxygenation

9. Beckmann Rearrangement

10. Benzilic Acid Rearrangement

11. Benzoin Condensation

12. Bergman Cyclization

13. Biginelli Reaction

14. Birch Reduction

15. Bischler–Napieralski Reaction

16. Brook Rearrangement

17. Brown Hydroboration

18. Bucherer–Bergs Reaction

19. Büchner Ring Expansion

20. Buchwald–Hartwig Amination

21. Burgess reagent

22. Cadiot–Chodkiewicz Coupling

23. Cannizzaro Reaction

24. Catellani Reaction

25. Chan–Lam C–X Coupling Reaction

26. Chapman Rearrangement

27. Chichibabin Pyridine Synthesis

28. Chugaev Elimination

29. Claisen Condensation

30. Claisen Rearrangement

31. Clemmensen Reduction

32. Cope Elimination

33. Cope Rearrangement

34. Corey–Bakshi–Shibata (CBS) Reduction

35. Corey−Chaykovsky Reaction

36. Corey−Fuchs Reaction

37. Curtius Rearrangement

38. Dakin Oxidation

39. Dakin−West Reaction

40. Darzens Condensation

41. de Mayo Reaction

42. Demjanov Rearrangement

43. Dess−Martin Periodinane Oxidation

44. Dieckmann Condensation

45. Diels–Alder Reaction

46. Dienone–Phenol Rearrangement

47. Dötz Reaction

48. Eschweiler–Clarke Reductive Amination

49. Favorskii Rearrangement

50. Ferrier Carbocyclization

51. Ferrier Glycal Allylic Rearrangement

52. Fischer Indole Synthesis

53. Friedel–Crafts Reaction

54. Friedländer Quinoline Synthesis

55. Fries Rearrangement

56. Gabriel Synthesis

57. Gewald Aminothiophene Synthesis

58. Glaser Coupling

59. Gould–Jacobs Reaction

60. Grignard Reaction

61. Grob Fragmentation

62. Hajos–Wiechert Reaction

63. Hantzsch Dihydropyridine Synthesis

64. Heck Reaction

65. Henry Nitroaldol Reaction

66. Hiyama Reaction

67. Hofmann Elimination

68. Hofmann Rearrangement

69. Hofmann–Löffler–Freytag Reaction

70. Horner–Wadsworth–Emmons Reaction

71. Houben-Hoesch Reaction

72. Hunsdiecker-Borodin Reaction

73. Jacobsen–Katsuki Epoxidation

74. Jones Oxidation

75. Julia–Kocienski Olefination

76. Julia–Lythgoe Olefination

77. Knoevenagel Condensation

78. Knorr Pyrazole Synthesis

79. Koenig–Knorr Glycosidation

80. Krapcho Reaction

81. Kröhnke Pyridine Synthesis

82. Kumada Reaction

83. Lawesson’s Reagent

84. Leuckart–Wallach Reaction

85. Lossen Rearrangement

86. McMurry Coupling

87. Mannich Reaction

88. Markovnikov’s Rule

89. Martin’s Sulfurane Dehydrating Reagent

90. Meerwein–Ponndorf–Verley Reduction

91. Meisenheimer Complex

92. Meyer–Schuster Rearrangement

93. Michael Addition

94. Michaelis-Arbuzov Phosphonate Synthesis

95. Minisci Reaction

96. Mitsunobu Reaction

97. Miyaura Borylation

98. Morita–Baylis–Hillman Reaction

99. Mukaiyama Aldol Reaction

100. Mukaiyama Michael Addition

101. Mukaiyama Reagent

102. Nazarov Cyclization

103. Neber Rearrangement

104. Nef Reaction

105. Negishi Cross-Coupling Reaction

106. Newman-Kwart Rearrangement

107. Nicholas Reaction

108. Noyori Asymmetric Hydrogenation

109. Nozaki–Hiyama–Kishi Reaction

110. Olefin Metathesis

111. Oppenauer Oxidation

112. Overman Rearrangement

113. Paal–Knorr Pyrrole Synthesis

114. Parham Cyclization

115. Passerini Reaction

116. Paternó–Büchi Reaction

117. Pauson-Khand Reaction

118. Payne Rearrangement

119. Petasis Reaction

120. Peterson Olefination

121. Pictet–Spengler Tetrahydroisoquinoline Synthesis

122. Pinacol Rearrangement

123. Pinner Reaction

124. Polonovski Reaction

125. Polonovski–Potier Reaction

126. Prins Reaction

127. Pummerer Rearrangement

128. Ramberg–Bäcklund Reaction

129. Reformatsky Reaction

130. Ritter Reaction

131. Robinson Annulation

132. Sandmeyer Reaction

133. Schiemann Reaction

134. Schmidt Rearrangement

135. Shapiro Reaction

136. Sharpless Asymmetric Amino-hydroxylation

137. Sharpless Asymmetric Dihydroxylation

138. Sharpless Asymmetric Epoxidation

139. Simmons–Smith Reaction

140. Smiles Rearrangement

141. Sommelet–Hauser Rearrangement

142. Sonogashira Reaction

143. Stetter Reaction

144. Stevens Rearrangement

145. Stille Coupling

146. Strecker Amino Acid Synthesis

147. Suzuki–Miyaura Coupling

148. Swern Oxidation

149. Takai Reaction

150. Tebbe Reagent

151. Tsuji-Trost Reaction

152. Ugi Reaction

153. Ullmann Coupling

154. Vilsmeier-Haack Reaction

155. von Braun Reaction

156. Wacker Oxidation

157. Wagner–Meerwein Rearrangement

158. Williamson Ether Synthesis

159. Wittig Reaction

160. Wolff Rearrangement

161. Wolff–Kishner Reaction

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Tags: Li Jie Jack, Name Reactions, Collection, Detailed Mechanisms, Synthetic Applications