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 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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