【유기화학】 27강. 주요 반응 메커니즘 요약

27강. 주요 반응 메커니즘 요약

 

추천글 : 【유기화학】 유기화학 목차 

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출처 : DALL.E

 

1. acetoacetic ester synthesis

 

2. acyloin condensation

 

3. aldol addition

 

4. Aldol condensation 

 

5. Arbuzov reaction

 

6. Arndt-Eistert synthesis 

 

7. Aza-Cope rearrangement

 

8. azo coupling

 

9. Baeyer-Villiger oxidation

 

10. Baylis-Hillman reaction

 

11. Beckmann rearrangement

 

12. benzilic acid rearrangement

 

13. benzoin condensation 

 

14. Birch reduction 

 

15. Bischler-Napieralski reaction

 

16. boronic acid Mannich reaction

 

17. brown hydroboration 

 

18. Cannizzaro reaction 

 

19. Claisen condensation 

 

20. Claisen rearrangement 

 

21. Claisen-Schmidt reaction

 

22. Clemmensen reduction 

 

23. Cope elimination

 

24. Cope rearrangement

 

25. Corey-Posner-Whitesides-House Reaction

 

26. Corey-Seebach reaction

 

27. Cumene process 

 

28. Curtius rearrangement 

 

29. Darzens condensation 

 

30. Dess-Martin oxidation 

 

31. Diazotisation

 

32. Dieckmann condensation

 

33. Diels-Alder reaction

 

34. 1,3-dipolar cycloaddition 

 

35. Eschweiler-Clarke reaction 

 

36. Ester pyrolysis

 

37. Favorskii rearrangement 

 

38. Fischer esterification

 

39. Friedel-Crafts acylation

 

40. Friedel-Crafts alkylation

 

41. Fries rearrangement 

 

42. Gabriel synthesis 

 

43. Gattermann-Koch reaction 

 

44. 그롭 조각화(Grob fragmentation)

 

45. Grubbs reaction (Olefin metathesis)

 

46. Haloform reaction

 

47. Heck reaction 

 

48. Hell-Volhard-Zelinsky(HVZ) reaction

 

49. Hofmann elimination 

 

50. Horner-Wadsworth-Emmons reaction

 

51. Hundsdiecker reaction

 

52. Ireland-Claisen rearrangement

 

53. Johnson-Claisen rearrangement

 

54. Johnson-Corey-Chaykovsky reaction

 

55. Jones oxidation

 

56. Knoevenagel condensation

 

57. Kochi reaction 

 

58. Kolbe nitrile synthesis

 

59. Kolbe-Schmitt reaction 

 

60. malonic ester synthesis

 

61. Mannich reaction

 

62. McMurry reactoin

 

63. Meerwein-Ponndorf-Verley reduction

 

64. Michael addition

 

65. Mukaiyama aldol reaction

 

66. Negishi coupling 

 

67. oxy - Cope rearrangement

 

68. oxymercuration-demercuration reaction 

 

69. 가오존분해반응(ozonolysis) 

 

70. para-Claisen rearrangement

 

71. Payne epoxidation

 

72. Perkin's condensation

 

73. Pictet-Spengler reaction

 

74. Pinacol coupling reaction

 

75. Pinacol rearrangement

 

76. Pomeranz-Fritsch reaction

 

77. reductive amination reaction

 

78. Reimer-Tiemann reaction

 

79. Reformatsky reaction

  

80. ring expansion reaction

 

81. ring contraction reaction

 

82. ring formation reaction

 

83. ring opening reaction 

 

84. Ritter reaction

 

85. Robinson annulation

 

86. Rosenmund reduction

 

87. Sandmeyer reaction

 

88. Schmidt reaction

 

89. semi-pinacol rearrangement

 

90. Shapiro reaction 

 

91. Simmons-Smith reaction 

 

92. Stetter reaction

 

93. Strecker synthesis

 

94. Stork-Enamine reaction

 

95. Suzuki coupling

 

96. Swern oxidation

 

97. Tiffeneau-Demjanov rearrangement

 

98. tautomerization

 

99. Wilsmeier reaction

 

100. Williamson ether synthesis

 

101. Wittig reaction 

 

102. Wolff-Kishner reduction

 

103. Wolff rearrangement

 

104. Wurtz reaction

 

105. Wurtz-Fittig reaction

 

입력: 2022.02.02 17:55