NAME REACTIONS

By STEVEN HERNANDEZ

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–MÖHLAU 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 BÜCHNER–CURTIUS–SCHLOTTERBECK REACTION BÜCHNER 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 COREYCHAYKOVSKY 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 DELÉPINE AMINE SYNTHESIS DE MAYO REACTION DEMJANOV REARRANGEMENT TIFFENEAU–DEMJANOV REARRANGEMENT DESS–MARTIN OXIDATION DIECKMANN CONDENSATION DIELS–ALDER REACTION DIENONE–PHENOL REARRANGEMENT DI-S-METHANE REARRANGEMENT DOEBNER QUINOLINE SYNTHESIS DÖTZ REACTION DOWD–BECKWITH RING EXPANSION ERLENMEYERPLÖCHL AZLACTONE SYNTHESIS ESCHENMOSER–TANABE FRAGMENTATION ESCHWEILER–CLARKE REDUCTIVE ALKYLATION OF AMINES EVANS ALDOL REACTION FAVORSKII REARRANGEMENT AND QUASI-FAVORSKII REARRANGEMENT FEIST–BÉNARY FURAN SYNTHESIS FERRIER CARBOCYCLIZATION FERRIER GLYCAL ALLYLIC REARRANGEMENT FIESSELMANN THIOPHENE SYNTHESIS FISCHER INDOLE SYNTHESIS FISCHER OXAZOLE SYNTHESIS FLEMING–TAMAO OXIDATION TAMAOKUMADA OXIDATION FRIEDEL–CRAFTS REACTION FRIEDLÄNDER 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 HALLER–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–LÖFFLER–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 KRÖHNKE PYRIDINE SYNTHESIS KUMADA CROSS-COUPLING REACTION LAWESSON’S REAGENT LEUCKART–WALLACH REACTION LOSSEN REARRANGEMENT MCFADYEN–STEVENS REDUCTION MCMURRY COUPLING MACMILLAN CATALYST MANNICH REACTION MARSHALL BORONATE FRAGMENTATION MARTIN’S 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 SYNTHESIS MIDLAND REDUCTION MISLOW–EVANS REARRANGEMENT MITSUNOBU REACTION MIYAURA BORYLATION MOFFATT OXIDATION MONTGOMERY COUPLING MORGAN–WALLS REACTION PICTET–HUBERT REACTION MORI–BAN INDOLE SYNTHESIS MUKAIYAMA ALDOL REACTION MUKAIYAMA MICHAEL ADDITION MUKAIYAMA REAGENT MYERSSAITO CYCLIZATION NAZAROV CYCLIZATION NEBER REARRANGEMENT NEF REACTION NEGISHI CROSS-COUPLING REACTION NENITZESCU INDOLE SYNTHESIS NICHOLAS REACTION NICOLAOU DEHYDROGENATION NICOLAOU HYDROXY-DITHIOKETAL CYCLIZATION NICOLAOU HYDROXY-KETONE REDUCTIVE CYCLIC ETHER FORMATION NICOLAOU OXYSELENATION NOYORI ASYMMETRIC HYDROGENATION NOZAKI–HIYAMA–KISHI REACTION OPPENAUER OXIDATION OVERMAN REARRANGEMENT PAAL THIOPHENE SYNTHESIS PAAL–KNORR FURAN SYNTHESIS PARHAM CYCLIZATION PASSERINI REACTION PATERNӖBÜCHI REACTION PAUSON–KHAND CYCLOPENTENONE SYNTHESIS PAYNE REARRANGEMENT PECHMANN COUMARIN SYNTHESIS PERKIN REACTION PETASIS REACTION PETERSON OLEFINATION PICTET–GAMS ISOQUINOLINE SYNTHESIS PICTET–SPENGLER TETRAHYDROISOQUINOLINE SYNTHESIS PINACOL REARRANGEMENT PINNER REACTION POLONOVSKI REACTION POLONOVSKI–POTIER REARRANGEMENT POMERANZ–FRITSCH REACTION SCHLITTLER–MÜLLER MODIFICATION PRÉVOST TRANS-DIHYDROXYLATION WOODWARD CIS-DIHYDROXYLATION PRINS REACTION PSCHORR CYCLIZATION PUMMERER REARRANGEMENT RAMBERG–BÄCKLUND 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–SCHÖPF REACTION ROSENMUND REDUCTION RUBOTTOM OXIDATION RUPE REARRANGEMENT SAEGUSA OXIDATION SAKURAI ALLYLATION REACTION SANDMEYER REACTION SCHIEMANN REACTION SCHMIDT REACTION SCHMIDT’S 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 NEWMANKWART REACTION TRUCESMILE REARRANGEMENT SOMMELET REACTION SOMMELET–HAUSER REARRANGEMENT SONOGASHIRA REACTION STAUDINGER KETENE CYCLOADDITION STAUDINGER REDUCTION STERNBACH BENZODIAZEPINE SYNTHESIS STETTER REACTION STILL–GENNARI PHOSPHONATE REACTION STILLE COUPLING STILLE–KELLY REACTION STOBBE CONDENSATION STORK ENAMINE REACTION STRECKER AMINO ACID SYNTHESIS SUZUKI COUPLING SWERN OXIDATION TAKAI IODOALKENE SYNTHESIS TEBBE OLEFINATION PETASIS ALKENYLATION TEMPO-MEDIATED OXIDATION THORPEZIEGLER REACTION TSUJI–TROST ALLYLATION UGI REACTION ULLMANN REACTION VAN LEUSEN OXAZOLE SYNTHESIS VILSMEIER–HAACK REACTION VILSMEIER MECHANISM FOR ACID CHLORIDE FORMATION VINYLCYCLOPROPANECYCLOPENTENE 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