Organic Chemistry 100 Must-Know Mechanisms in pdf

 Organic Chemistry 100 Must-Know Mechanisms in pdf

this is the book Organic Chemistry 100 Must-Know Mechanisms in pdf written  by  Roman A. Valiulin  published  by de Gruyter ,2020 of professors of  science faculties  universities  .

   

Information about the book

Language of the book: English language

Book Title: Organic Chemistry 100 Must-Know Mechanisms

Scriptwriter: by Roman A. Valiulin

Year of printing: by Gruyter ,2020

File Format:PDF

Number of chapters: 100 CHAPTER

Number of pages: 251 pages

File Size: 15,70MB

Contents

1 Electrophilic Addition Mechanism 10

2 Nucleophilic Substitution Mechanism 12

3 Aromatic Electrophilic Substitution Mechanism 14

4 Aromatic Nucleophilic Substitution Mechanism 16

5 Aromatic Radical Nucleophilic Substitution Mechanism 18

6 Elimination Mechanism 22

7 Acyloin Condensation 26

8 Alkyne Zipper Reaction 28

9 Arbuzov Reaction 30

10 Arndt‒Eistert Synthesis 32

11 Baeyer‒Villiger Oxidation 34

12 Barton Decarboxylation 36

13 Baylis‒Hillman Reaction 38

14 Beckmann Rearrangement 40

15 Benzoin Condensation 42

16 Benzyne Mechanism 44

17 Bergman Cyclization 46

18 Birch Reduction 48

19 Bischler‒Napieralski Cyclization 50

20 Brown Hydroboration 52

21 Buchwald‒Hartwig Cross Coupling 54

22 Cannizzaro Reaction 56

23 Chan‒Evans‒Lam Cross Coupling 58

24 Chichibabin Amination 60

25 Claisen Condensation 62

26 Claisen Rearrangement 64

27 Cope Elimination 66

28 Cope Rearrangement 68

29 Criegee & Malaprade Oxidation 70

30 CuAAC 72

31 Curtius Rearrangement 74

32 Darzens Condensation 78

33 Dess‒Martin Oxidation 80

34 Diazotization (Diazonium Salt) 82

35 Diels‒Alder Cycloaddition 84

36 Di‒π‒Methane Rearrangement 86

37 Favorskii Rearrangement 88

38 Fischer Indole Synthesis 90

39 Friedel‒Crafts Acylation & Alkylation 92

40 Gabriel Synthesis 94

41 Gewald Reaction 96

42 Glaser–Eglinton–Hay Coupling 98

43 Grignard Reaction 100

44 Grob Fragmentation 102

45 Haloform Reaction 104

46 Heck Cross Coupling 106

47 Hell–Volhard–Zelinsky Reaction 108

48 Hiyama Cross Coupling 110

49 Hofmann Elimination 112

50 Horner–Wadsworth–Emmons Olefination 114

51 Jones Oxidation 116

52 Kucherov Reaction 118

53 Kumada Cross Coupling 120

54 Ley–Griffith Oxidation 122

55 Liebeskind–Srogl Cross Coupling 124

56 Mannich Reaction 126

57 McMurry Coupling 128

58 Meerwein–Ponndorf–Verley Reduction 130

59 Michael Addition 132

60 Minisci Reaction 134

61 Mitsunobu Reaction 136

62 Miyaura Borylation 138

63 Mukaiyama RedOx Hydration 140

64 Nazarov Cyclization 142

65 Nef Reaction 144

66 Negishi Cross Coupling 146

67 Norrish Type I & II Reaction 148

68 Olefin (Alkene) Metathesis 150

69 Oppenauer Oxidation 154

70 Ozonolysis 156

71 Paal–Knorr Syntheses 158

72 Paternò–Büchi Reaction 162

73 Pauson–Khand Reaction 164

74 Peptide (Amide) Coupling 166

75 Pictet–Spengler Reaction 170

76 Pinacol–Pinacolone Rearrangement 172

77 Polonovski Reaction 174

78 Prilezhaev Epoxidation 176

79 Prins Reaction 178

80 Pummerer Rearrangement 180

81 Ramberg–Bäcklund Rearrangement 182

82 Reformatsky Reaction 184

83 Robinson Annulation 186

84 Shapiro Reaction 188

85 Sonogashira Cross Coupling 190

86 Staudinger Reaction 192

87 Steglich Esterification 194

88 Stille Cross Coupling 196

89 Suzuki Cross Coupling 198

90 Swern Oxidation 200

91 Ugi Reaction 202

92 Ullmann Aryl–Aryl Coupling 204

93 Upjohn Dihydroxylation 206

94 Vilsmeier–Haack Reaction 208

95 Wacker Oxidation 210

96 Wagner–Meerwein Rearrangement 212

97 Weinreb Ketone Synthesis 214

98 Wittig Reaction 216

99 Wohl–Ziegler Reaction 218

100 Wolff–Kishner Reduction 220

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