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synthesis fischer oxazole synthesis fischer peptide synthesis fischer phenylhydrazine and oxazone reaction fischer glycosidation fischer hepp rearrangement fischer speier esterification fischer tropsch synthesis fleming tamao oxidation flood reaction folin ciocalteu reagent formox process forster reaction forster decker method fowler process franchimont reaction frankland synthesis frankland duppa reaction fráter seebach alkylation free radical halogenation freund reaction friedel crafts acylation friedel crafts alkylation friedländer synthesis fries rearrangement fritsch buttenberg wiechell rearrangement fujimoto belleau reaction fujiwara moritani reaction fukuyama coupling fukuyama indole synthesis fukuyama reduction g edit gabriel ethylenimine method gabriel synthesis gabriel colman rearrangement gabriel isoquinoline synthesis gallagher hollander degradation gassman indole synthesis gastaldi synthesis gattermann aldehyde synthesis gattermann koch reaction gattermann reaction geminal halide hydrolysis gewald reaction gibbs phthalic anhydride process gilman reagent glaser coupling glycol cleavage goldberg reaction gomberg bachmann reaction gomberg bachmann hey reaction gomberg radical reaction gould jacobs reaction graebe ullmann synthesis grignard degradation griesbaum coozonolysis grignard reaction grob fragmentation grubbs catalyst in olefin metathesis grundmann aldehyde synthesis gryszkiewicz trochimowski and mccombie method guareschi thorpe condensation guerbet reaction gutknecht pyrazine synthesis h edit hajos parrish eder sauer wiechert reaction haller bauer reaction haloform reaction halogen addition reaction halohydrin formation reaction hammick reaction hammond principle or hammond postulate hantzsch pyrrole synthesis hantzsch dihydropyridine synthesis hantzsch pyridine synthesis hantzsch pyridine synthesis gattermann skita synthesis guareschi thorpe condensation knoevenagel fries modification hantzsch collidin synthesis harries ozonolysis haworth methylation haworth synthesis hay coupling hayashi rearrangement heck reaction hegedus indole synthesis helferich method hell volhard zelinsky halogenation hemetsberger indole synthesis hemetsberger knittel synthesis henkel reaction raecke process henkel process henry reaction kamlet reaction herz reaction herz compounds herzig meyer alkimide group determination heumann indigo synthesis hiyama coupling hydration reaction hydroamination hydrodesulfurization hydrogenolysis hydrosilylation hinsberg indole synthesis hinsberg oxindole synthesis hinsberg reaction hinsberg separation hinsberg sulfone synthesis hirao coupling hoch campbell ethylenimine synthesis hock rearrangement hofmann bromamide reaction hofmann degradation exhaustive methylation hofmann elimination hofmann isonitrile synthesis carbylamine reaction hofmann product hofmann rearrangement hofmann löffler reaction löffler freytag reaction hofmann löffler freytag reaction hofmann martius rearrangement hofmann s rule hofmann sand reaction homo rearrangement of steroids hooker reaction horner wadsworth emmons reaction hoesch reaction hosomi sakurai reaction houben fischer synthesis hudlicky fluorination huisgen cycloaddition hunsdiecker reaction hunsdiecker borodin reaction hurd mori 1 2 3 thiadiazole synthesis hurtley reaction hydroboration hydrocarbon cracking hydrohalogenation i edit indium mediated allylation ing manske procedure ipso substitution ireland claisen rearrangement isay reaction ishikawa reagent trans cis isomerism ivanov reagent ivanov reaction j edit jacobsen epoxidation jacobsen rearrangement janovsky reaction japp klingemann reaction japp maitland condensation jocic reaction johnson claisen rearrangement johnson corey chaykovsky reaction 26 27 jones oxidation 28 29 jordan ullmann goldberg synthesis julia olefination julia lythgoe olefination 30 k edit kabachnik fields reaction kharasch sosnovsky reaction keck asymmetric allylation ketimine mannich reaction ketone halogenation kiliani fischer synthesis kindler reaction kishner cyclopropane synthesis knoevenagel condensation knorr pyrazole synthesis knorr pyrrole synthesis knorr quinoline synthesis koch haaf reaction kochi reaction koenigs knorr reaction kolbe electrolysis kolbe nitrile synthesis kolbe schmitt reaction kornblum oxidation kornblum delamare rearrangement kostanecki acylation kowalski ester homologation krapcho decarboxylation krische allylation kröhnke aldehyde synthesis kröhnke oxidation kröhnke pyridine synthesis kucherov reaction kuhn winterstein reaction kulinkovich reaction kumada coupling l edit larock indole synthesis lawesson s reagent lebedev process lehmstedt tanasescu reaction leimgruber batcho indole synthesis letts nitrile synthesis leuckart reaction leuckart thiophenol reaction leuckart wallach reaction leuckart amide synthesis levinstein process ley griffith oxidation ley oxidation lieben iodoform reaction haloform reaction liebeskind srogl coupling liebig melamine synthesis lindlar catalyst lobry de bruyn van ekenstein transformation lombardo methylenation lossen rearrangement lucas reagent luche reduction m edit maillard reaction madelung synthesis malaprade reaction periodic acid oxidation malonic ester synthesis mannich reaction markó lam deoxygenation markovnikov s rule markownikoff rule markownikow rule marschalk reaction martinet dioxindole synthesis mcdougall monoprotection mcfadyen stevens reaction mcmurry reaction meerwein arylation meerwein ponndorf verley reduction meisenheimer rearrangement meissenheimer complex menshutkin reaction metal ion catalyzed σ bond rearrangement mesylation merckwald asymmetric synthesis metallo ene reaction methylation meyer hartmann reaction meyer reaction meyer synthesis meyer schuster rearrangement michael addition michael addition michael system michael condensation michaelis arbuzov reaction midland alpine borane reduction mignonac reaction milas hydroxylation of olefins minisci reaction mislow evans rearrangement mitsunobu reaction miyaura borylation modified wittig claisen tandem reaction molisch s test mozingo reduction mukaiyama aldol addition mukaiyama reaction mukaiyama hydration myers asymmetric alkylation n edit nametkin rearrangement narasaka prasad reduction nazarov cyclization reaction neber rearrangement nef reaction negishi coupling negishi zipper reaction nenitzescu indole synthesis nenitzescu reductive acylation newman kwart rearrangement nicholas reaction niementowski quinazoline synthesis niementowski quinoline synthesis nierenstein reaction nih shift ninhydrin test nitroaldol reaction nitrone olefin 3 2 cycloaddition normant reagents noyori asymmetric hydrogenation nozaki hiyama kishi reaction nucleophilic acyl substitution o edit ohira bestmann reaction olah reagent olefin metathesis oppenauer oxidation orton rearrangement ostromyslenskii reaction ostromisslenskii reaction overman rearrangement oxidative decarboxylation oxo synthesis oxy cope rearrangement oxymercuration oxidation of alcohols to carbonyl compounds ozonolysis p edit paal knorr pyrrole synthesis paal knorr synthesis paneth technique passerini reaction paternò büchi reaction pauson khand reaction payne rearrangement pechmann condensation pechmann pyrazole synthesis pellizzari reaction pelouze synthesis peptide synthesis perkin alicyclic synthesis perkin reaction perkin rearrangement perkow reaction petasis reaction petasis reagent peterson olefination peterson reaction petrenko kritschenko piperidone synthesis pfau plattner azulene synthesis pfitzinger reaction pfitzner moffatt oxidation phosphonium coupling photosynthesis piancatelli rearrangement pictet gams isoquinoline synthesis pictet hubert reaction pictet spengler tetrahydroisoquinoline synthesis pictet spengler reaction piloty robinson pyrrole synthesis pinacol coupling reaction pinacol rearrangement pinner amidine synthesis pinner method for ortho esters pinner reaction pinner triazine synthesis pinnick oxidation piria reaction polonovski reaction pomeranz fritsch reaction ponzio reaction prato reaction prelog strain prevost reaction prileschajew reaction prilezhaev reaction prins reaction prinzbach synthesis protecting group pschorr reaction pummerer rearrangement purdie methylation irvine purdie methylation q edit quelet reaction r edit ramberg bäcklund reaction raney nickel rap stoermer condensation raschig phenol process rauhut currier reaction racemization reductive amination reductive dehalogenation of halo ketones reed reaction reformatsky reaction also transliterated as reformatskii reaction 31 reilly hickinbottom rearrangement reimer tiemann reaction reissert indole synthesis reissert reaction reissert compound reppe synthesis retropinacol rearrangement rieche formylation riemschneider thiocarbamate synthesis riley oxidations ring closing metathesis ring opening metathesis ritter reaction 32 33 robinson annulation robinson gabriel synthesis robinson schopf reaction rosenmund reaction rosenmund reduction rosenmund von braun synthesis roskamp reaction rothemund reaction rupe rearrangement rubottom oxidation ruff fenton degradation ruzicka large ring synthesis s edit saegusa ito oxidation sakurai reaction salol reaction sandheimer sandmeyer diphenylurea isatin synthesis sandmeyer isonitrosoacetanilide isatin synthesis sandmeyer reaction sanger reagent saponification sarett oxidation schiemann reaction 18 schiff reaction schiff test schlenk equilibrium schlosser modification schlosser variant schmidlin ketene synthesis schmidt degradation schmidt reaction scholl reaction schorigin shorygin reaction shorygin reaction wanklyn reaction schotten baumann reaction seliwanoff s test semidine rearrangement semmler wolff reaction seyferth gilbert homologation shapiro reaction sharpless asymmetric dihydroxylation sharpless epoxidation 34 sharpless oxyamination or aminohydroxylation shenck ene reaction shi epoxidation shiina esterification shiina macrolactonization or shiina lactonization sigmatropic reaction simmons smith reaction simonini reaction simonis chromone cyclization simons process skraup chinolin synthesis skraup reaction smiles rearrangement s n ar nucleophilic aromatic substitution s n 1 s n 2 s n i solvolysis sommelet reaction sonn müller method sonogashira coupling sørensen formol titration staedel rugheimer pyrazine synthesis stahl oxidation staudinger reaction staudinger synthesis steglich esterification stephen aldehyde synthesis stetter reaction stevens rearrangement stieglitz rearrangement stille coupling stobbe condensation stollé synthesis stork acylation stork enamine alkylation strecker amino acid synthesis strecker degradation strecker sulfite alkylation strecker synthesis stereocontrolled 1 2 addition to carbonyl groups suzuki coupling swain equation swarts reaction swern oxidation t edit tamao oxidation tafel rearrangement takai olefination tebbe olefination ter meer reaction thiele reaction thiol yne reaction thorpe reaction tiemann rearrangement tiffeneau ring enlargement reaction tiffeneau demjanov rearrangement tischtschenko reaction tishchenko reaction tishchenko claisen reaction tollens reagent transfer hydrogenation trapp mixture transesterification traube purine synthesis truce smiles rearrangement tscherniac einhorn reaction tschitschibabin reaction tsuji trost reaction tsuji wilkinson decarbonylation reaction twitchell process tyrer sulfonation process u edit ugi reaction ullmann reaction upjohn dihydroxylation urech cyanohydrin method urech hydantoin synthesis v edit van leusen reaction van slyke determination varrentrapp reaction vilsmeier reaction vilsmeier haack reaction voight amination volhard erdmann cyclization von braun amide degradation von braun reaction von richter cinnoline synthesis von richter reaction w edit wacker tsuji oxidation wagner jauregg reaction wagner meerwein rearrangement walden inversion wallach rearrangement weerman degradation weinreb ketone synthesis weitz scheffer epoxidation wenker ring closure wenker synthesis wessely moser rearrangement westphalen lettré rearrangement wharton reaction whiting reaction wichterle reaction widman stoermer synthesis wilkinson catalyst willgerodt rearrangement willgerodt kindler reaction williamson ether synthesis winstein reaction wittig reaction wittig rearrangement 1 2 wittig rearrangement 2 3 wittig rearrangement wittig horner reaction wohl degradation wohl aue reaction wohler synthesis wohl ziegler reaction wolffenstein böters reaction wolff rearrangement wolff kishner reduction woodward cis hydroxylation woodward hoffmann rule wulff dötz reaction wurtz coupling wurtz reaction wurtz fittig reaction y edit yamada okamoto purine synthesis yamaguchi esterification z edit zaitsev s rule zeisel determination zerevitinov determination zerewitinoff determination ziegler condensation ziegler method zimmermann reaction zincke disulfide cleavage zincke nitration zincke reaction zincke suhl reaction zinin reduction see also edit wikimedia commons has media related to organic reactions stigler s law of eponymy name reaction list of organic compounds list of inorganic compounds named inorganic compounds list of biomolecules list of minerals references edit treibs wilhelm schmidt harry 1927 zur katalytischen dehydrierung hydro aromatischer verbindungen catalytic dehydrogenation of hydroaromatic compounds berichte der deutschen chemischen gesellschaft in german 60 10 2335 2341 doi 10 1002 cber 187600901134 alder kurt nobel theo 1943 über die anlagerung von azodicarbonsäure ester an aldehyde substituting additions ii addition of azodicarboxylic esters to aldehydes berichte der deutschen chemischen gesellschaft in german 76 1 54 57 doi 10 1002 cber 19430760106 alder kurt pascher franz schmitz andreas 1943 über die anlagerung von maleinsäure anhydrid und azodicarbonsäure ester an einfach ungesättigte koh an einfach ungesättigte kohlenwasserstoffe zur kenntnis von substitutionsvorgängen in der allyl stellung substituting additions i addition of maleic anhydride and azodicarboxylic esters to singly unsaturated hydrocarbons substitution processes in the allyl position berichte der deutschen chemischen gesellschaft 76 1 27 53 doi 10 1002 cber 19430760105 alder kurt schmidt carl heinz 1943 über die kondensation des furans und seiner homologen mit α β ungesättigten ketonen und aldehyden aufbau von di tri und tetraketonen der fettreihe substituting additions iii condensation of furan and its homologs with α β unsaturated ketones and aldehydes synthesis of di tri and tetraketones of the aliphatic series berichte der deutschen chemischen gesellschaft in german 76 3 183 205 doi 10 1002 cber 19430760302 aston j g greenburg r b 1942 alpha bromo secondary alkyl ketones i reaction with sodium alcoholates a new synthesis of tertiary acids by rearrangement 1 2 journal of the american chemical society 62 10 2590 2595 doi 10 1021 ja01867a003 wang zerong 2010 comprehensive organic name reactions and reagents doi 10 1002 9780470638859 conrr026 isbn 97804717...