Comprehensive Organic Name Reactions and Reagents: 3 Volume Set

With its coverage of 701 organic name reactions and reagents, this three–volume set is the largest, most up–to–date major reference work of its kind.  It offers students and professional chemists a valuable resource for conducting experiments and performing a broad range of applications, from pharmaceuticals to plastics to pesticides.  Each reaction listing is clearly organized into uniform sections that allow readers to quickly gather the information they need to conduct their own experimental procedures
Comprehensive Organic Name Reactions and Reagents offers several features that help readers gather information quickly and conduct their experiments successfully:Chemical abbreviations list the abbreviation, the chemical’s full name, its structure, and page referencesSchematic reaction index offers a quick overview of each reactionReaction summaries provide basic information about each name reactionReaction type summaries categorize and organize all related name reactions according to the type of transformation (e.g., oxidation, reduction, synthesis of alkenes, etc.)

Spis treści:
Preface.
Acknowledgments.
Autobiography.
Chemical Abbreviations.
PART ONE.
1. Abnormal Claisen Rearrangement.
2. Acetoacetic Ester Condensation.
3. Acetoacetic Ester Synthesis.
4. Acyloin Condensation.
5. Acyloin Rearrangement.
6. Adkins Catalyst.
7. Ainley and King Synthesis.
8. Akabori Amino Acid Reaction.
9. Albright–Goldman Oxidation.
10. Alder Ene Reaction.
11. Alder–Rickert Reaction.
12. Aldol Reaction and Aldol Condensation.
13. Algar–Flynn–Oyamada (AFO) Reaction.
14. Alkene Metathesis.
15. Allan–Robinson Condensation.
16. Allylic Rearrangement.
17. Amadori Rearrangement.
18. Andrussow Process.
19. Angeli–Remini Reaction.
20. ANRORC Rearrangement.
21. Anschutz Anthracen e Synthesis.
22. Appel Reaction.
23. Arens–Van Dorp Reaction.
24. Arndt–Eistert Synthesis.
25. Asinger Reaction.
26. Aston–Greenburg Rearrangement.
27. Atherton–Todd Reaction.
28. Auwers–Skita Rule.
29. Aza–Claisen Rearrangement.
30. Baddeley Isomerization.
31. Baeyer Diarylmethane Synthesis.
32. Baeyer–Drewson Reaction.
33. Baeyer Indole Synthesis.
34. Baeyer Oxindole Synthesis.
35. Baeyer Pyridine Synthesis.
36. Baeyer–Villiger Oxidation.
37. Bailey Peptide Synthesis.
38. Bakelite Process.
39. Baker–Ollis Sydnones Synthesis.
40. Baker–Venkataraman Rearrangement.
41. Ball–Goodwin–Morton Oxidation.
42. Bally–Scholl Reaction.
43. Balsohn Alkylation.
44. Balz–Schiemann Reaction.
45. Bamberger Rearrangement.
46. Bamford–Stevens Reaction.
47. Barbier Reaction.
48. Barbier–Wieland Degradation.
49. Bardhan Sengupta Synthesis.
50. Bargellini Condensation.
51. Bart Reaction.
52. Bartoli Indole Synthesis.
53. Barton Decarboxylation.
54. Barton Deoxygenation.
55. Barton Reaction.
56. Barton–Kellogg Olefination.
57. Barton–Zard Pyrrole Synthesis.
58. Batcho–Leimgruber Indole Synthesis.
59. Baudisch Reaction.
60. Baumann–Fromm Thiophene Synthesis.
61. Baumgarten α–Amino Ketone Synthesis.
62. Baylis–Hillman Reaction.
63. B´echamp Reduction.
64. Beckmann Rearrangement and Beckmann Fragmentation.
65. Bedoukian Halogenation.
66. B´ehal–Sommelet Rearrangement.
67. Beirut Reaction.
68. Bellus–Claisen Rearrangement.
69. B´enary Reaction.
70. Benkeser Reduction.
71. Benzidine Rearrangement.
72. Benzilic Acid Rearrangement.
73. Benzoin Condensation.
74. Bergius Process.
75. Bergman Cyclization.
76. Bergmann Degradation.
77. Bergmann–Stern Azlactone Synth esis.
78. Bergmann–Zervas Peptide Synthesis.
79. Bernthsen Reaction.
80. Berti Olefination.
81. Bertram–Walbaum Reaction.
82. Betti Reaction.
83. Biginelli Reaction.
84. Birch Reduction.
85. Birckenbach–Goubeau Halogenation.
86. Birnbaum–Simonini Reaction.
87. Bischler Reaction.
88. Bischler–Napieralski Isoquinoline Synthesis.
89. Black Rearrangement.
90. Blaise Ketone Synthesis.
91. Blaise Reaction.
92. Blanc Chloromethylation.
93. Blanc Rule.
94. Blomquist Cyclic Ketone Synthesis.
95. Bobbitt Reaction.
96. Bodroux Amide Synthesis.
97. Bodroux–Chichibabin Reaction.
98. B¨oeseken Oxidation.
99. Bogert–Cook Synthesis.
100. Bohn–Schmidt Reaction.
101. Boord Olefin Synthesis.
102. Borsche–Berkhout Reaction.
103. Borsche–Drechsel Reaction.
104. Borsche–Koelsch Cinnoline Synthesis.
105. Bougault Reaction.
106. Boulton–Katritzky Rearrangement.
107. Bourgel Alkyne Synthesis.
108. Bouveault Aldehyde Synthesis.
109. Bouveault–Blanc Reduction.
110. Boyland–Sims Oxidation.
111. Bradsher Cyclization.
112. Bradsher Cycloaddition.
113. Bradsher Pyridinium Salt Synthesis.
114. Brandi–Guarna Reaction.
115. Breckpot β–Lactam Synthesis.
116. Bredt’s Rule.
117. Brook Rearrangement.
118. Brown Hydroboration.
119. Bruckner Isoquinoline Synthesis.
120. Bucherer Carbazole Synthesis.
121. Bucherer Reaction.
122. Bucherer–Bergs Hydantoin Synthesis.
123. B¨uchner Ring Expansion.
124. B¨uchner–Curtius–Schlotterbeck Reaction.
125. Buchwald Indoline Synthesis.
126. Buchwald–Hartwig Amination.
127. Burton Trifluoromethylation.
128. Cadogan–Sundberg Indole Synthesis.
129. Caglioti Reaction.
130. Cahours–Hofmann Reaction.
131. Camps Reaction.
132. Cannizzaro Reaction.
133. Car boni–Lindsey Reaction.
134. Carroll Rearrangement.
135. Castro Indole Synthesis.
136. Castro–Stephens Coupling.
137. Chan Rearrangement.
138. Chapman Rearrangement.
139. Chichibabin Amination.
140. Chichibabin Pyridine Synthesis.
141. Chretien–Longi Reaction.
142. Chugaev Reaction.
143. Ciamician–Dennstedt Reaction.
144. Claisen Rearrangement.
145. Claisen–Schmidt Condensation.
146. Clauson–Kaas Reaction.
147. Clay–Kinnear–Perren Condensation.
148. Clayton–Jensen Chlorophosphonation.
149. Clemmensen Reduction.
150. Cohen Reductive Lithiation.
151. Combes Quinoline Synthesis.
152. Conrad–Limpach Quinoline Synthesis.
153. Cope Elimination.
154. Cope Rearrangement.
155. Corey–Bakshi–Shibata Reduction.
156. Corey–Chaykovsky Epoxidation.
157. Corey–Fuchs Reaction.
158. Corey–Gilman–Ganem Oxidation.
159. Corey–Kim Oxidation.
160. Corey–Kwiatkowski Reaction.
161. Corey–Link Reaction.
162. Corey–Schmidt Oxidation.
163. Corey–Suggs Oxidation.
164. Corey–Winter Olefination.
165. Cornforth Rearrangement.
166. Craig 2–Bromo–Pyridine Synthesis.
167. Cram’s Rule.
168. Criegee Glycol Oxidation.
169. Criegee Ozonolysis.
170. Criegee Rearrangement.
171. Crum–Brown–Gibson Substitution Rule.
172. Curtius Rearrangement.
173. [m+n(+. . . )] Cycloaddition.
174. [2+2] Cycloaddition.
175. Dakin Reaction.
176. Dakin–West Reaction.
177. Danheiser Annulation.
178. Darzens Condensation.
179. Darzens Halogenation.
180. Darzens Olefin Acylation.
181. Darzens–Nenitzescu Reaction.
182. Davidson Oxazole Cyclization.
183. de Mayo Reaction.
184. Decker–Becker Secondary Amine Synthesis.
185. Del´epine Reaction.
186. Demjanov Rearrangement.
187. Dess–Mart in Periodinane Oxidation.
188. D–Homo Rearrangement.
189. Dieckmann Condensation.
190. Diels–Alder Reaction.
191. Diels–Reese Reaction.
192. Dienol–Benzene Rearrangement.
193. Dienone–Phenol Rearrangement.
194. Dimroth Rearrangement.
195. Di–Π–Methane Rearrangement.
196. 1,3–Dipolar Cycloaddition.
197. Doebner Reaction.
198. Doebner–Miller Reaction.
199. Doering–Moore–Skattebøl Reaction.
200. Dotz Benzannulation.
201. Dowd–Beckwith Ring Expansion.
202. Duff Reaction.
203. Dutt–Wormall Reaction.
204. Eastwood Olefination.
205. Eder Reaction.
206. Edman Degradation.
207. Eglinton Coupling.
208. Ehrlich–Sachs Reaction.
209. Einhorn Acylation.
210. Einhorn–Brunner Reaction.
211. Eisleb Alkylation.
212. Elbs Persulfate Oxidation.
213. Elbs Reaction.
214. Eltekoff Hydrolysis.
215. Emde Degradation.
216. Emmert Reaction.
217. Erlenmeyer–plochl Azlactone Synthesis.
218. Eschenmoser Coupling.
219. Eschenmoser Fragmentation.
220. Eschweiler–Clarke Methylation.
221. Ester Pyrolysis.
222. E´ tard Reaction.
223. Evans Aldol Reaction.
224. Favorskii Rearrangement.
225. Favorskii–Babayan Reaction.
226. Feist–Benary Reaction.
227. Fenton Reaction.
228. Ferrier Reaction.
229. Ferrier–II Rearrangement.
230. F´etizon Oxidation.
231. Finkelstein Reaction.
232. Fischer Carbene Complexes.
233. Fischer Indole Synthesis.
234. Fischer Oxazole Synthesis.
235. Fischer Phenylhydrazine Synthesis.
236. Fischer Phenylhydrazone and Osazone Synthesis.
237. Fischer–Helferich Glycosylation.
238. Fischer–Hepp Rearrangement.
239. Fischer–Speier Esterification.
240. Fischer–Tropsch Synthesis.
241. Fleming–Tamao Oxidation.
242. Flood Reaction.
243. Forster Reaction.
244. Franchimont Condensation.
245. Frankland Reaction.
246. Fr´ater–Seebach Alkylation.
247. Freund Reaction.
248. Friedel–Crafts Acylation.
249. Friedel–Crafts Alkylation.
250. Friedl¨ander Condensation.
251. Fries Rearrangement.
252. Fritsch–Buttenberg–Wiechell Rearrangement.
253. Fujimoto–Belleau Reaction.
254. Fukuyama Amine Synthesis.
255. Fukuyama Indole Synthesis.
256. F¨urstner Indole Synthesis.
257. Gabriel Primary Amine Synthesis.
258. Gabriel Reaction.
259. Gabriel–Colman Rearrangement.
260. Garner Aldehyde.
261. Gassman Indole Synthesis.
262. Gassman Oxindole Synthesis.
263. Gassman Reaction.
264. Gattermann Aldehyde Synthesis.
265. Gattermann Reaction.
266. Gattermann–Koch Formylation.
267. Gewald Reaction.
268. Ghosez Cyclization.
269. Ghosez Keteniminium–Olefin Cyclization.
270. Gibbs–Wohl Naphthalene Oxidation.
271. Gilman–Cason Ketone Synthesis.
272. Gilman–Speeter Reaction.
273. Gomberg Free Radical Reaction.
274. Gomberg–Bachmann Pinacol Synthesis.
275. Gomberg–Bachmann Reaction.
276. Gould–Jacobs Reaction.
277. Graebe–Ullmann Synthesis.
278. Gr¨anacher Synthesis.
279. Gribble Reductive Amination.
280. Griess Diazotization.
281. Grignard Degradation.
282. Grignard Reaction.
283. Grob Fragmentation.
284. Grosheintz–Fischer–Reissert Aldehyde Synthesis.
285. Grundmann Aldehyde Synthesis.
286. Gryszkiewicz–Trochimowski and Mccombie Fluorination.
287. Guareschi Reaction.
288. Guerbet Condensation.
289. Gutknecht Condensation.
PART TWO.
290. Hajos–Parrish–Eder–Sauer–Wiechert Reaction.
291. Haller–Bauer Cleavage.
292. Hammick Reaction.
293. Hansley–Prelog Acyloin Condensation.
294. Hantzsch Dihydropyridine Synthesis.
295. Hantzsch Pyrrole Synthesis.
296. Hantzsch Thiazole Synthesis.
297. Hass–Bender Oxidation.
298. Haworth Methylation.
299. Haworth Synthesis.
300. Hayashi Rearrangement.
301. Heck Reaction.
302. Hegedus Indole Synthesis.
303. Helferich Condensation.
304. Helferich Glycosylation.
305. Hell–Volhard–Zelinsky Reaction.
306. Hemetsberger Indole Synthesis.
307. Henkel Reaction.
308. Henry Reaction.
309. Herbst–Engel Transamination.
310. Heron Rearrangement.
311. Herz Reaction.
312. Heumann Indigo Process.
313. Heyns Rearrangement.
314. Hilbert–Johnson Reaction.
315. Hinsberg Oxindole Synthesis.
316. Hinsberg Reaction.
317. Hinsberg Sulfone Synthesis.
318. Hinsberg Thiophene Synthesis.
319. Hiyama Coupling.
320. Hoch–Campbell Reaction.
321. Hock Rearrangement.
322. Hofer–Moest Reaction.
323. Hofmann Degradation.
324. Hofmann Elimination.
325. Hofmann Isonitrile Synthesis.
326. Hofmann Rule.
327. Hofmann–Loffler–Freytag Reaction.
328. Hofmann–Martius Rearrangement.
329. Hofmann–Sand Reaction.
330. Hooker Oxidation.
331. Horenstein–P¨ahlicke Reaction.
332. Horner–Wadsworth–Emmons Olefination.
333. Hosomi–Sakurai Allylation.
334. Houben–Hoesch Reaction.
335. Houdry Cracking Process.
336. Huisgen Pyrrole Synthesis.
337. Hunsdiecker Condensation.
338. Hunsdiecker Reaction.
339. Hydroformylation.
340. Iodolactonization.
341. Irvine–Purdie Methylation.
342. Jacobsen Rearrangement.
343. Jacobsen–Katsuki Epoxidation.
344. Janovsky Reaction.
345. Japp–Klingemann Fischer Indole Synthesis.
346. Japp–Klingemann Reaction.
347. Japp–Maitland Condensation.
348. Johnson Orthoester Claisen Rearrangement.
349. Jones Oxidation.
350. Jourdan–Ullmann Reaction.
351. Julia Olefination.
352. Jul i´a–Colonna Asymmetric Epoxidation.
353. Kabachnik–Fields Reaction.
354. Kahne Glycosylation.
355. Keck Allylation.
356. Keck Macrolactonization.
357. Kemp Elimination.
358. Kennedy Oxidative Cyclization.
359. Kiliani–Fischer Cyanohydrin Synthesis.
360. Kishner Decomposition.
361. Knoevenagel Condensation.
362. Knoevenagel Diazotization Method.
363. Knorr Pyrazole Synthesis.
364. Knorr Pyrrole Synthesis.
365. Knorr Quinoline Synthesis.
366. Koch–Haaf Carboxylation.
367. Kochi Reaction.
368. Koenigs–Knorr Reaction.
369. Kolbe Electrolysis.
370. Kolbe Nitrile Synthesis.
371. Kolbe–Schmidt Reaction.
372. Kondrat’eva Pyridine Synthesis.
373. Kornblum Oxidation.
374. Kornblum–Delamare Rearrangement.
375. Kostanecki–Robinson Reaction.
376. Kowalski Ester Homologation.
377. Krapcho Decarboxylation.
378. Kriewitz Condensation.
379. Kr¨ohnke Pyridine Synthesis.
380. Kuhn–Roth Oxidation.
381. Kuhn–Winterstein Reduction.
382. Kulinkovich Cyclopropanation.
383. Kutscheroff Acetylene Hydration.
384. Lander Rearrangement.
385. Larock Indole Synthesis.
386. Lawesson’s Reagent.
387. Lebedev Process.
388. Lehmstedt–Tanasescu Reaction.
389. Lemieux–Johnson Oxidation.
390. Leuckart Reaction.
391. Leuckart Thiophenol Synthesis.
392. Levinstein Process.
393. Lieben Iodoform Reaction.
394. Liebeskind–Srogl Cross–Coupling.
395. Lindlar Hydrogenation.
396. Lobry de Bruyn–Alberda van Ekenstein Transformation.
397. Lombardo Methylenation.
398. Lossen Rearrangement.
399. Luche Reaction.
400. Luche Reduction.
401. MacDonald–Fischer Degradation.
402. Madelung Indole Synthesis.
403. Maillard Reaction.
404. Maitland–Japp Reaction.
405. Majetich Annulation.
406. Malaprade Reaction.
407. Malonic Ester Synthesis.