命名反应

Abbreviations

Alder ene reaction

Aldol condensation

Algar-Flynn-Oyamada reaction

Allan-Robinson reaction

Appel reaction

Arndt-Eistert homologation

Baeyer-Villiger oxidation

Baker-Venkataraman rearrangement

Bamberger rearrangement

Bamford-Stevens reaction

Barbier coupling reaction

Bargellini reaction

Bartoli indole synthesis

Barton radical decarboxylation

Barton-McCombie deoxygenation

Barton nitrite photolysis

Barton-Zard reaction

Batcho-Leimgruber indole synthesis

Baylis-Hillman reaction

Beckmann rearrangement

Beirut reaction

Benzilic acid rearrangement

Benzoin condensation

Bergman cyclization.

Biginelli pyrimidone synthesis

Birch reduction

Bischler-Mthlau indole synthesis

Bischler-Napieralski reaction

Blaise reaction

Blanc chloromethylation

Blum aziridine synthesis

Boekelheide reaction

Boger pyridine synthesis

Borch reductive amination

Borsche-Drechsel cyclization

Boulton-Katritzky rearrangement

Bouveault aldehyde synthesis

Bouveault-Blanc reduction

Boyland-Sims oxidation

Bradsher reaction

Brook rearrangement

Brown hydroboration

Bucherer carbazole synthesis

Bucherer reaction

Bucherer-Bergs reaction

Buchner-Curtius-Schlotterbeck reaction

Buchner method of ring expansion

Buchwald-Hartwig C-N bond and C-O bond formation reactions

Burgess dehydrating reagent

Cadiot--Chodkiewicz coupling

Camps quinolinol synthesis

Cannizzaro dispropotionation

Carroll rearrangement

Castro-Stephens coupling

Chan alkyne reduction

Chan-Lam coupling reaction

Chapman rearrangement

Chichibabin pyridine synthesis

Chugaev reaction

Ciamician-Dennsted rearrangement

Claisen condensation

Claisen isoxazole synthesis

Claisen rearrangement

Abnormal Claisen rearrangement

Eschenmoser-Claisen amide acetal rearrangement

Ireland--Claisen (silyl ketene acetal) rearrangement

Johnson-Claisen (orthoester) rearrangement

Clemmensen reduction

Combes quinoline synthesis

Conrad-Limpach reaction

Cope elimination reaction

Cope rearrangement

Oxy-Cope rearrangement

Anionic oxy-Cope rearrangement

Corey-Bakshi-Shibata (CBS) reduction

Corey--Chaykovsky reaction

Corey-Fuchs reaction

Corey-Kim oxidation

Corey-Nicolaou macrolactonization

Corey-Seebach dithiane reaction

Corey-Winter olefin synthesis

Criegee glycol cleavage

Criegee mechanism of ozonolysis

Curtius rearrangement

Dakin oxidation

Dakin-West reaction

Danheiser annulation

Darzens glycidic ester condensation

Davis chiral oxaziridine reagent

Delepine amine synthesis

de Mayo reaction

Demjanov rearrangement

Tiffeneau-Demjanov rearrangement

Dess-Martin oxidation

Dieckmann condensation

Diels-Alder reaction

Dienone-phenol rearrangement

Di-π-methane rearrangement

Doebner quinoline synthesis

Dptz reaction

Dowd-Beckwith ring expansion

Edenmeyer-Plochl azlactone synthesis

Eschenmoser-Tanabe fragmentation

Eschweiler-Clarke reductive alkylation of amines

Evans aldol reaction

Favorskii rearrangement and quasi-Favorskii rearrangement

Feist-Benary furan synthesis

Ferrier carbocyclization

Ferrier glycal allylic rearrangement

Fiesselmann thiophene synthesis

Fischer indole synthesis

Fischer oxazole synthesis

Fleming-Tamao oxidation

Tamao-Kumada oxidation

Friedel-Crafts reaction

Friedlander quinoline synthesis

Fries rearrangement

Fukuyama amine synthesis

Fukuyama reduction

Gabriel synthesis

Ing-Manske procedure

Gabriel-Colman rearrangement

Gassman indole synthesis

Gattermann-Koch reaction

Gewald aminothiophene synthesis

Glaser coupling

Eglinton coupling

Gomberg-Bachmann reaction

Gould-Jacobs reaction

Grignard reaction

Grob fragmentation

Guareschi-Thorpe condensation

Hajos-Wiechert reaction

Hailer-Bauer reaction

Hantzsch dihydropyridine synthesis

Hantzsch pyrrole synthesis

Heck reaction

Heteroaryl Heck reaction

Hegedus indole synthesis

Hell-Volhard-Zelinsky reaction

Henry nitroaldol reaction

Hinsberg synthesis of thiophene derivatives

Hiyama cross-coupling reaction

Hiyama-Denmark cross-coupling reaction

Hofmann rearrangement

Hofmann-Loffler-Freytag reaction

Horner-Wadsworth-Emmons reaction

Houben-Hoesch synthesis

Hunsdiecker-Borodin reaction

Hurd-Mori 1,2,3-thiadiazole synthesis

Jacobsen-Katsuki epoxidation

Japp--Klingemann hydrazone synthesis

Jones oxidation

Julia-Kocienski olefination

Julia-Lythgoe olefination

Kahne--Crich glycosidation

Keck macrolactonization

Knoevenagel condensation

Knorr pyrazole synthesis

Paal-Knorr pyrrole synthesis

Koch-Haaf carbonylation

Koenig-Knorr glycosidation

Kolbe-Schmitt reaction

Kostanecki reaction

Krohnke pyridine synthesis

Kumada cross-coupling reaction

Lawessons reagent

Leuckart-Wallach reaction

Lossen rearrangement

McFadyen-Stevens reduction

McMurry coupling

MacMillan catalyst

Mannich reaction

Marshall boronate fragmentation

Martins sulfurane dehydrating reagent

Masamune-Roush conditions

Meerwein-Ponndorf-Verley reduction

Meisenheimer complex

[1,2]-Meisenheimer rearrangement

[2,3]-Meisenheimer rearrangement

Meth-Cohn quinoline synthesis

Meyers oxazoline method

Meyer-Schuster rearrangement

Michael addition

Michaelis-Arbuzov phosphonate syathesis

Midland reduction

Mislow-Evans rearrangement

Mitsunobu reaction

Miyaura borylation

Moffatt oxidation

Montgomery coupling

Morgan-Walls reaction

Pictet-Hubert reaction

Moil-Ban indole synthesis

Mukaiyama aldol reaction

Mukaiyama Michael addition

Mukaiyama reagent

Myers-Saito cyclization

Nazarov cyclization

Neber rearrangement

Nef reaction

Negishi cross-coupling reaction

Nenitzescu indole synthesis

Nicholas reaction

Nicolaou dehydrogenation

Nicolaou hydroxy-dithioketal cyelization

Nicolaou hydroxy-ketone reduction

Nicolaou oxyselenation

Noyori asymmetric hydrogenation

Nozaki-Hiyama-Kishi reaction

Oppenauer oxidation

Overman rearrangement

Paal thiophene synthesis

Paal-Knorr furan synthesis

Parham cyclization

Passerini reaction

Patemt-Buchi reaction

Pauson-Khand cyclopentenone synthesis

Payne rearrangement

Pechmann coumarin synthesis

Perkin reaction

Petasis reaction

Peterson olefination

Pictet--Gams isoquinoline synthesis

Pictet-Spengler tetrahydroisoquinoli

Pinacol rearrangement

Pinner reaction

Polonovski reaction

Polonovski-Potier rearrangement

Pomeranz-Fritsch reaction

Schlittler-M011er modification

Prevost trans-dihydroxylation

Woodward cis-dihydroxylation

Prins reaction

Pschorr cyclization

Pummerer rearrangement

Ramberg-Baicklund reaction

Reformatsky reaction

Regitz diazo synthesis

Reimer-Tiemann reaction

Reissert aldehyde synthesis

Reissert indole synthesis

Ring-closing metathesis

Ritter reaction

Robinson annulation

Robinson-Gabriel synthesis

Robinson-Schopf reaction

Rosenmund reduction

Rubottom oxidation

Rupe rearrangement

Saegusa oxidation

Sakurai allylation reaction

Sandmeyer reaction

Schiemann reaction

Schmidt reaction

Schmidts trichloroacetimidate glycosidation reaction

Shapiro reaction

Sharpless asymmetric amino hydroxylation

Sharpless asymmetric epoxidation

Sharpless asymmetric dihydroxylation

Sharpless olefin synthesis

Simmons-Smith reaction

Skraup quinoline synthesis

Doebner-von Miller reaction

Smiles rearrangement

Newman-Kwart reaction

Truce-Smile rearrangement

Sommelet reaction

Sommelet-Hauser rearrangement

Sonogashira reaction

Staudinger ketene cycloaddition

Staudinger reduction

Stembach benzodiazepine synthesis

Stetter reaction

Still-Gennari phosphonate reaction

Stille coupling

Stille-Kelly reaction

Stobbe condensation

Stork enamine reaction

Strecker amino acid synthesis

Suzuki coupling.

Swem oxidation

Takai iodoalkene synthesis

Tebbe olefination

Petasis alkenylation

TEMPO-mediated oxidation

Thorpe-Ziegler reaction

Tsuji-Trost allylation

Ugi reaction

Ullmann reaction

van Leusen oxazole synthesis

Vilsmeier-Haack reaction

Vilsmeier mechanism for acid chloride formation

Vinylcyclopropane-cyclopentene rearrangement

von Braun reaction

Wacker oxidation

Wagner-Meerwein rearrangement

Weiss-Cook reaction

Wharton oxygen transposition reaction

Willgerodt-Kindler reaction

Wittig reaction

Schlosser modification of the Wittig reaction

[ 1,2]-Wittig rearrangement

[2,3]-Wittig rearrangement

Wohl-Ziegler reaction

Wolff rearrangement

Wolff-Kishner reduction

Yamaguchi esterification

Zincke reaction

Subject Index

The third edition contains major improvements over the previous two editions. I have updated references. Each reaction is now supplemented with two to three representative examples in synthesis to showcase its synthetic utility. As Emil Fi-scher stated：“Science is not an abstraction; but as a product of human endeavor it is inseparably bound up in its development with the personalities and fortunes of those who dedicate themselves to it .” To that end， I added biographical sketches Furthemore， I have significantly beefed up the subject index to help the reader na-vigate the book more easily.