有機化學：100個反應機理

反應機理001
1親電加成機理(electrophilic addition mechanism)002
2親核取代機理(nucleophilic substitution mechanism)004
3芳香親電取代機理(aromatic electrophilic substitution mechanism)006
4芳香親核取代機理(aromatic nucleophilic substitution mechanism)008
5芳香自由基親核取代機理(aromatic radical nucleophilic substitution mechanism)010
6消除機理(elimination mechanism)014
7酮醇縮合(acyloin condensation)018
8炔烴拉鏈反應(alkyne zipper reaction)020
9阿爾布佐夫反應(Arbuzov reaction)022
10阿恩特－艾斯特爾特合成(Arndt-Eistert synthesis)024
11拜耳-維利格氧化(Baeyer-Villiger oxidation)026
12巴頓脫羧(Barton decarboxylation)028
13貝里斯-希爾曼反應(Baylis-Hillman reaction)030
14貝克曼重排(Beckmann rearrangement)032
15安息香縮合(benzoin condensation)034
16苯炔機理(benzyne mechanism)036
17伯格曼環(huán)化(Bergman cyclization)038
18伯奇還原(Birch reduction)040
19比施勒-納皮耶拉爾斯基環(huán)化(Bischler-Napieralski cyclization)042
20布朗硼氫化(Brown hydroboration)044
21布赫瓦爾德-哈特維希交叉偶聯(lián)(Buchwald-Hartwig cross coupling)046
22坎尼扎羅反應(Cannizzaro reaction)048
23陳-埃文斯-蘭交叉偶聯(lián)(Chan-Evans-Lam cross coupling)050
24齊齊巴賓氨基化(Chichibabin amination)052
25克萊森縮合(Claisen condensation)054
26克萊森重排(Claisen rearrangement)056
27柯普消除(Cope elimination)058
28柯普重排(Cope rearrangement)060
29克里奇氧化和馬拉普拉德氧化(Criegee & Malaprade oxidation)062
30銅催化疊氮-炔環(huán)加成(copper-catalyzed azide-alkyne cycloaddition, CuAAC)064
31柯提斯重排(Curtius rearrangement)066
32達森縮合(Darzens condensation)070
33戴斯-馬丁氧化(Dess-Martin oxidation)072
34重氮化反應(diazotization)074
35狄爾斯-阿爾德環(huán)加成(Diels-Alder cycloaddition)076
36雙-π-甲烷重排(di-π-methane rearrangement)078
37法沃爾斯基重排(Favorskii rearrangement)080
38費歇爾吲哚合成(Fischer indole synthesis)082
39傅-克酰基化和傅-克烷基化(Friedel-Crafts acylation & alkylation)084
40蓋布瑞爾合成(Gabriel synthesis)086
41格瓦爾德反應(Gewald reaction)088
42格拉澤-埃格林頓-海偶聯(lián)(Glaser-Eglinton-Hay coupling)090
43格氏反應(Grignard reaction)092
44格羅布裂解(Grob fragmentation)094
45鹵仿反應(haloform reaction)096
46赫克交叉偶聯(lián)(Heck cross coupling)098
47黑爾-福爾哈德-澤林斯基反應(Hell-Volhard-Zelinsky reaction)100
48檜山交叉偶聯(lián)(Hiyama cross coupling)102
49霍夫曼消除(Hofmann elimination)104
50霍納-沃茲沃斯-埃蒙斯烯烴化(Horner-Wadsworth-Emmons olefination)106
51瓊斯氧化(Jones oxidation)108
52庫切羅夫反應(Kucherov reaction)110
53熊田交叉偶聯(lián)(Kumada cross coupling)112
54萊伊-格里菲斯氧化(Ley-Griffith oxidation)114
55利貝斯金德-斯羅格爾交叉偶聯(lián)(Liebeskind-Srogl cross coupling)116
56曼尼希反應(Mannich reaction)118
57麥克默里偶聯(lián)(McMurry coupling)120
58麥爾外因-龐多夫-維利還原(Meerwein-Ponndorf-Verley reduction)122
59邁克爾加成(Michael addition)124
60米尼希反應(Minisci reaction)126
61光延反應(Mitsunobu reaction)128
62宮浦硼化(Miyaura borylation)130
63向山氧化還原水合(Mukaiyama RedOx hydration)132
64納扎羅夫環(huán)化(Nazarov cyclization)134
65尼夫反應(Nef reaction)136
66根岸交叉偶聯(lián)(Negishi cross coupling)138
67諾里什Ⅰ型和Ⅱ型反應(Norrish type Ⅰ & Ⅱ reaction)140
68烯烴復分解[olefin (alkene) metathesis]142
69歐芬腦爾氧化(Oppenauer oxidation)146
70臭氧分解(ozonolysis)148
71帕爾-克諾爾合成(Paal-Knorr syntheses)150
72帕特羅-布奇反應(Paternò-Büchi reaction)154
73保森-坎德反應(Pauson-Khand reaction)156
74肽（酰胺）偶聯(lián)[peptide (amide) coupling]158
75皮克特-斯彭格勒反應(Pictet-Spengler reaction)162
76頻哪醇-頻哪酮重排(pinacol-pinacolone rearrangement)164
77波羅諾夫斯基反應(Polonovski reaction)166
78普里萊扎耶夫環(huán)氧化(Prilezhaev epoxidation)168
79普林斯反應(Prins reaction)170
80普默勒重排(Pummerer rearrangement)172
81蘭伯格-貝克倫德重排(Ramberg-B?cklund rearrangement)174
82雷福爾馬茨基反應(Reformatsky reaction)176
83羅賓遜環(huán)化(Robinson annulation)178
84夏皮羅反應(Shapiro reaction)180
85薗頭交叉偶聯(lián)反應(Sonogashira cross coupling)182
86施陶丁格反應(Staudinger reaction)184
87斯特格里奇酯化(Steglich esterification)186
88施蒂勒交叉偶聯(lián)反應(Stille cross coupling)188
89鈴木交叉偶聯(lián)反應(Suzuki cross coupling)190
90斯文氧化(Swern oxidation)192
91烏吉反應(Ugi reaction)194
92烏爾曼芳基-芳基偶聯(lián)(Ullmann aryl-aryl coupling)196
93厄普約翰雙羥基化反應(Upjohn dihydroxylation)198
94維爾斯邁爾-哈克反應(Vilsmeier-Haack reaction)200
95瓦克氧化(Wacker oxidation)202
96瓦格納-麥爾外因重排(Wagner-Meerwein rearrangement)204
97溫勒伯酮合成(Weinreb ketone synthesis)206
98維蒂希反應(Wittig reaction)208
99沃爾-齊格勒反應(Wohl-Ziegler reaction)210
100沃爾夫-凱惜納還原(Wolff-Kishner reduction)212
參考書目與文獻214
中文索引229
英文索引233