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n friedel crafts reaction fujimoto belleau reaction fujiwara moritani reaction fukuyama coupling gabriel colman rearrangement gattermann reaction glaser coupling grignard reaction grignard reagent hammick reaction heck reaction henry reaction heterogeneous metal catalyzed cross coupling high dilution principle hiyama coupling homologation reaction horner wadsworth emmons reaction hydrocyanation hydrovinylation hydroxymethylation ivanov reaction johnson corey chaykovsky reaction julia olefination julia kocienski olefination kauffmann olefination knoevenagel condensation knorr pyrrole synthesis kolbe schmitt reaction kowalski ester homologation kulinkovich reaction kumada coupling liebeskind srogl coupling malonic ester synthesis mannich reaction mcmurry reaction meerwein arylation methylenation michael reaction minisci reaction mizoroki heck vs reductive heck nef isocyanide reaction nef synthesis negishi coupling nierenstein reaction nitro mannich reaction nozaki hiyama kishi reaction olefin conversion technology olefin metathesis palladium nhc complex passerini reaction peterson olefination pfitzinger reaction piancatelli rearrangement pinacol coupling reaction prins reaction quelet reaction ramberg bäcklund reaction rauhut currier reaction reformatsky reaction reimer tiemann reaction rieche formylation ring closing metathesis robinson annulation sakurai reaction seyferth gilbert homologation shapiro reaction sonogashira coupling stetter reaction stille reaction stollé synthesis stork enamine alkylation suzuki reaction takai olefination thermal rearrangement of aromatic hydrocarbons thorpe reaction ugi reaction ullmann reaction wagner jauregg reaction weinreb ketone synthesis wittig reaction wurtz reaction wurtz fittig reaction zincke suhl reaction homologation reactions arndt eistert reaction hooker reaction kiliani fischer synthesis kowalski ester homologation methoxymethylenetriphenylphosphorane seyferth gilbert homologation wittig reaction olefination reactions bamford stevens reaction barton kellogg reaction boord olefin synthesis chugaev elimination cope reaction corey winter olefin synthesis dehydrohalogenation elimination reaction grieco elimination hofmann elimination horner wadsworth emmons reaction hydrazone iodination julia olefination julia kocienski olefination kauffmann olefination mcmurry reaction peterson olefination ramberg bäcklund reaction shapiro reaction takai olefination wittig reaction carbon heteroatom bond forming reactions azo coupling bartoli indole synthesis boudouard reaction cadogan sundberg indole synthesis diazonium compound esterification grignard reagent haloform reaction hegedus indole synthesis hurd mori 1 2 3 thiadiazole synthesis kharasch sosnovsky reaction knorr pyrrole synthesis leimgruber batcho indole synthesis mukaiyama hydration nenitzescu indole synthesis oxymercuration reaction reed reaction schotten baumann reaction ullmann condensation williamson ether synthesis yamaguchi esterification degradation reactions barbier wieland degradation bergmann degradation edman degradation emde degradation gallagher hollander degradation hofmann rearrangement hooker reaction isosaccharinic acid marker degradation ruff degradation strecker degradation von braun amide degradation weerman degradation wohl degradation organic redox reactions acyloin condensation adkins peterson reaction akabori amino acid reaction alcohol oxidation algar flynn oyamada reaction amide reduction andrussow process angeli rimini reaction aromatization autoxidation baeyer villiger oxidation barton mccombie deoxygenation bechamp reduction benkeser reaction bergmann degradation birch reduction bohn schmidt reaction bosch reaction bouveault blanc reduction boyland sims oxidation cannizzaro reaction carbonyl reduction clemmensen reduction collins oxidation corey itsuno reduction corey kim oxidation corey winter olefin synthesis criegee oxidation dakin oxidation davis oxidation deoxygenation dess martin oxidation dna oxidation elbs persulfate oxidation emde degradation eschweiler clarke reaction étard reaction fischer tropsch process fleming tamao oxidation fukuyama reduction ganem oxidation glycol cleavage griesbaum coozonolysis grundmann aldehyde synthesis haloform reaction hydrogenation hydrogenolysis hydroxylation jones oxidation kiliani fischer synthesis kolbe electrolysis kornblum oxidation kornblum delamare rearrangement leuckart reaction ley oxidation lindgren oxidation lipid peroxidation lombardo methylenation luche reduction markó lam deoxygenation mcfadyen stevens reaction meerwein ponndorf verley reduction methionine sulfoxide miyaura borylation mozingo reduction noyori asymmetric hydrogenation omega oxidation oppenauer oxidation oxygen rebound mechanism ozonolysis parikh doering oxidation pinnick oxidation prévost reaction reduction of nitro compounds reductive amination riley oxidation rosenmund reduction rubottom oxidation sabatier reaction sarett oxidation selenoxide elimination shapiro reaction sharpless asymmetric dihydroxylation epoxidation of allylic alcohols sharpless epoxidation sharpless oxyamination stahl oxidation staudinger reaction stephen aldehyde synthesis swern oxidation transfer hydrogenation wacker process wharton reaction whiting reaction wohl aue reaction wolff kishner reduction wolffenstein böters reaction zinin reaction rearrangement reactions 1 2 rearrangement 1 2 wittig rearrangement 2 3 sigmatropic rearrangement 2 3 wittig rearrangement achmatowicz reaction alkyne zipper reaction allen millar trippett rearrangement allylic rearrangement alpha ketol rearrangement amadori rearrangement arndt eistert reaction aza cope rearrangement baker venkataraman rearrangement bamberger rearrangement banert cascade beckmann rearrangement benzilic acid rearrangement bergman cyclization bergmann degradation boekelheide reaction brook rearrangement buchner ring expansion carroll rearrangement chan rearrangement claisen rearrangement cope rearrangement corey fuchs reaction cornforth rearrangement criegee rearrangement curtius rearrangement demjanov rearrangement di π methane rearrangement dimroth rearrangement divinylcyclopropane cycloheptadiene rearrangement dowd beckwith ring expansion reaction electrocyclic reaction ene reaction enyne metathesis favorskii reaction favorskii rearrangement ferrier carbocyclization ferrier rearrangement fischer hepp rearrangement fries rearrangement fritsch buttenberg wiechell rearrangement gabriel colman rearrangement group transfer reaction halogen dance rearrangement hayashi rearrangement hofmann rearrangement hofmann martius rearrangement ireland claisen rearrangement jacobsen rearrangement kornblum delamare rearrangement kowalski ester homologation lobry de bruyn van ekenstein transformation lossen rearrangement mcfadyen stevens reaction mclafferty rearrangement meyer schuster rearrangement mislow evans rearrangement mumm rearrangement myers allene synthesis nazarov cyclization reaction neber rearrangement newman kwart rearrangement overman rearrangement oxy cope rearrangement pericyclic reaction piancatelli rearrangement pinacol rearrangement pummerer rearrangement ramberg bäcklund reaction ring expansion and contraction ring closing metathesis rupe reaction schmidt reaction semipinacol rearrangement seyferth gilbert homologation sigmatropic reaction skattebøl rearrangement smiles rearrangement sommelet hauser rearrangement stevens rearrangement stieglitz rearrangement thermal rearrangement of aromatic hydrocarbons tiffeneau demjanov rearrangement vinylcyclopropane rearrangement wagner meerwein rearrangement wallach rearrangement weerman degradation westphalen lettré rearrangement willgerodt rearrangement wolff rearrangement ring forming reactions 1 3 dipolar cycloaddition annulation azide alkyne huisgen cycloaddition baeyer emmerling indole synthesis bartoli indole synthesis bergman cyclization biginelli reaction bischler möhlau indole synthesis bischler napieralski reaction blum ittah aziridine synthesis bobbitt reaction bohlmann rahtz pyridine synthesis borsche drechsel cyclization bucherer carbazole synthesis bucherer bergs reaction cadogan sundberg indole synthesis camps quinoline synthesis chichibabin pyridine synthesis cook heilbron thiazole synthesis cycloaddition darzens reaction davis beirut reaction de kimpe aziridine synthesis debus radziszewski imidazole synthesis dieckmann condensation diels alder reaction feist benary synthesis ferrario ackermann reaction fiesselmann thiophene synthesis fischer indole synthesis fischer oxazole synthesis friedländer synthesis gewald reaction graham reaction hantzsch pyridine synthesis hegedus indole synthesis hemetsberger indole synthesis hofmann löffler reaction hurd mori 1 2 3 thiadiazole synthesis iodolactonization isay reaction jacobsen epoxidation johnson corey chaykovsky reaction knorr pyrrole synthesis knorr quinoline synthesis kröhnke pyridine synthesis kulinkovich reaction larock indole synthesis madelung synthesis nazarov cyclization reaction nenitzescu indole synthesis niementowski quinazoline synthesis niementowski quinoline synthesis paal knorr synthesis paternò büchi reaction pechmann condensation petrenko kritschenko piperidone synthesis pictet spengler reaction pomeranz fritsch reaction prilezhaev reaction pschorr cyclization reissert indole synthesis ring closing metathesis robinson annulation sharpless epoxidation simmons smith reaction skraup reaction urech hydantoin synthesis van leusen reaction wenker synthesis cycloaddition 1 3 dipolar cycloaddition 4 4 photocycloaddition 4 3 cycloaddition 6 4 cycloaddition alkyne trimerisation aza diels alder reaction azide alkyne huisgen cycloaddition bradsher cycloaddition cheletropic reaction conia ene reaction cyclopropanation diazoalkane 1 3 dipolar cycloaddition diels alder reaction enone alkene cycloadditions hexadehydro diels alder reaction intramolecular diels alder cycloaddition inverse electron demand diels alder reaction ketene cycloaddition mccormack reaction metal centered cycloaddition reactions nitrone olefin 3 2 cycloaddition oxo diels alder reaction ozonolysis pauson khand reaction povarov reaction prato reaction retro diels alder reaction staudinger synthesis trimethylenemethane cycloaddition vinylcyclopropane 5 2 cycloaddition wagner jauregg reaction heterocycle forming reactions algar flynn oyamada reaction allan robinson reaction auwers synthesis bamberger triazine synthesis banert cascade barton zard reaction bernthsen acridine synthesis bischler napieralski reaction bobbitt reaction boger pyridine synthesis borsche drechsel cyclization bucherer carbazole synthesis bucherer bergs reaction chichibabin pyridine synthesis cook heilbron thiazole synthesis diazoalkane 1 3 dipolar cycloaddition einhorn brunner reaction erlenmeyer plöchl azlactone and amino acid synthesis feist benary synthesis fischer oxazole synthesis gabriel colman rearrangement gewald reaction hantzsch ester hantzsch pyridine synthesis herz reaction knorr pyrrole synthesis kröhnke pyridine synthesis lectka enantioselective beta lactam synthesis lehmstedt tanasescu reaction niementowski quinazoline synthesis nitrone olefin 3 2 cycloaddition paal knorr synthesis pellizzari reaction pictet spengler reaction pomeranz fritsch reaction prilezhaev reaction robinson gabriel synthesis stollé synthesis urech hydantoin synthesis wenker synthesis wohl aue reaction v t e concepts in organic chemistry aromaticity covalent bonding functional groups nomenclature organic compounds organic reactions organic synthesis publications spectroscopy stereochemistry list of organic compounds v t e compounds of carbon with other elements in the periodic table ch che cli cbe cb cc cn co cf cne cna cmg cal csi cp cs ccl car ck cca csc cti cv ccr cmn cfe cco cni ccu czn cga cge cas cse cbr ckr crb csr cy czr cnb cmo ctc cru crh cpd cag ccd cin csn csb cte ci cxe ccs cba clu chf cta cw cre cos cir cpt cau chg ctl cpb cbi cpo cat rn fr cra lr rf db csg bh hs mt ds rg cn nh fl mc lv ts og cla cce cpr cnd cpm csm ceu cgd ctb cdy cho cer ctm cyb cac cth cpa cu cnp cpu cam ccm cbk ccf ces fm md no legend chemical bonds to carbon core organic chemistry many uses in chemistry academic research no widespread use bond unknown v t e branches of chemistry glossary of chemical formulae list of biomolecules list of inorganic compounds periodic table analytical calorimetry characterization chromatography gc hplc crystallography electroanalytical methods elemental analysis instrumental chemistry mass spectrometry ei icp maldi separation process spectroscopy ir raman uv vis nmr titration wet chemistry theoretical computational chemistry mathematical chemistry molecular modelling molecular mechanics molecular dynamics molecular geometry vsepr theory quantum chemistry physical chemical kinetics chemical physics molecular physics chemical thermodynamics cryochemistry electrochemistry spectroelectrochemistry photoelectrochemistry equilibrium chemistry femtochemistry interface and colloid science micromeritics mechanochemistry microwave chemistry photochemistry sonochemistry spectroscopy spin chemistry structural chemistry surface science thermochemistry inorganic ceramic chemistry cluster chemistry coordination chemistry magnetochemistry organometallic chemistry organolanthanide chemistry solid state chemistry organic dynamic covalent chemistry enantioselective synthesis fullerene chemistry organic reactions organic synthesis petrochemistry physical organic chemistry polymer chemistry retrosynthetic analysis stereochemistry alkane stereochemistry total synthesis semisynthesis biological biochemistry molecular biology cell biology bioinorganic chemistry bioorganic chemistry bioorganometallic chemistry biophysical chemistry chemical biology bioorthogonal chemistry clinical chemistry medicinal chemistry pharmacology neurochemistry interdisciplinarity nuclear chemistry radiochemistry radiation chemistry actinide 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