RODD'S CHEMISTRY OF CARBON COMPOUNDS,: AROMATIC COMPOUNDS
THE DIELS–ALDER CYCLOADDITION REACTION IN THE CONTEXT OF DOMINO PROCESSES CASCADES NOT INITIATED BY DIELS–ALDER REACTION CASCADES GENERATING A DIENE IONIC GENERATION OF A DIENE THROUGH WESSELY OXIDATION OF PHENOLS THROUGH IONIC CYCLIZATION THROUGH DEPROTONATION OF AN ALKENE THROUGH ELIMINATION REACTIONS THROUGH ALLYLATION PERICYCLIC GENERATION OF A DIENE THROUGH ELECTROCYCLIZATION THROUGH BENZOCYCLOBUTENE RING OPENING THROUGH ELECTROCYCLIC RING CLOSURE THROUGH CYCLOADDITION OR RETROCYCLOADDITION THROUGH SIGMATROPIC REACTIONS PHOTOCHEMICAL GENERATION OF A DIENE METAL-MEDIATED GENERATION OF A DIENE CASCADES GENERATING A DIENOPHILE IONIC GENERATION OF A DIENOPHILE THROUGH HIMBERT CYCLOADDITIONS THROUGH BENZYNE FORMATION THROUGH WESSELY OXIDATION PERICYCLIC GENERATION OF A DIENOPHILE THROUGH CYCLOADDITION/RETROCYCLOADDITION THROUGH SIGMATROPIC REARRANGEMENT PROXIMITY-INDUCED DIELS–ALDER REACTIONS DIELS–ALDER AS THE INITIATOR OF A CASCADE PERICYCLIC REACTIONS OCCURRING IN THE WAKE OF A DIELS–ALDER REACTION CASCADES FEATURING DIELS–ALDER/DIELS–ALDER PROCESSES CASCADES FEATURING DIELS–ALDER/RETRO-DIELS–ALDER PROCESSES [4+2] CYCLOADDITION WITH SUBSEQUENT DESATURATION DIELS–ALDER REACTIONS WITH CONCOMITANT IONIC STRUCTURAL REARRANGEMENTS PAIRINGS OF DIELS–ALDER REACTIONS WITH STRUCTURAL FRAGMENTATIONS COMBINING A DIELS–ALDER REACTION WITH IONIC CYCLIZATION CONCLUSIONS DOMINO REACTIONS INCLUDING [2+2], [3+2], OR [5+2] CYCLOADDITIONS DOMINO [2+2] CYCLOADDITIONS CYCLOADDITION OF AN ENAMINONE AND -DIKETONE WITH FRAGMENTATION CYCLOADDITION OF YNOLATE ANIONS FOLLOWED BY DIECKMANN CONDENSATION/MICHAEL REACTION CYCLOADDITION CASCADE INVOLVING BENZYNE–ENAMIDE CYCLOADDITION OR A FISCHER CARBENE COMPLEX CYCLOADDITIONS WITH REARRANGEMENT CYCLOADDITION OF AN AZATRIENE FOLLOWED BY COPE REARRANGEMENT CYCLOADDITION OF A PROPARGYLIC ETHER AND PROPARGYLIC THIOETHER FOLLOWED BY [3,3]-SIGMATROPIC REARRANGEMENT [3,3]-SIGMATROPIC REARRANGEMENT OF PROPARGYLIC ESTER AND PROPARGYLIC ACETATE FOLLOWED BY CYCLOADDITION CYCLOADDITION OF A KETENE FOLLOWED BY ALLYLIC REARRANGEMENT ALLYL MIGRATION IN YNAMIDES FOLLOWED BY CYCLOADDITION 1,3-MIGRATION IN PROPARGYL BENZOATES FOLLOWED BY CYCLOADDITION DOMINO [3+2] CYCLOADDITIONS CYCLOADDITIONS WITH NITRONES, NITRONATES, AND NITRILE OXIDES REACTION TO GIVE A NITRONE FOLLOWED BY CYCLOADDITION CYCLOADDITION WITH A NITRONE AND SUBSEQUENT REACTION REACTION TO GIVE A NITRONATE FOLLOWED BY CYCLOADDITION REACTION TO GIVE A NITRILE OXIDE FOLLOWED BY CYCLOADDITION CYCLOADDITION WITH A NITRILE OXIDE AND SUBSEQUENT REACTION CYCLOADDITIONS WITH CARBONYL YLIDES REACTION OF AN Æ-DIAZO COMPOUND TO GIVE A CARBONYL YLIDE FOLLOWED BY CYCLOADDITION REACTION OF AN ALKYNE TO GIVE A CARBONYL YLIDE FOLLOWED BY CYCLOADDITION CYCLOADDITIONS WITH AZOMETHINE YLIDES CYCLOADDITIONS WITH AZOMETHINE IMINES CYCLOADDITIONS WITH AZIDES REACTION TO GIVE AN AZIDO-SUBSTITUTED ALKYNE FOLLOWED BY CYCLOADDITION CYCLOADDITION OF AN AZIDE AND SUBSEQUENT REACTION DOMINO [5+2] CYCLOADDITIONS CYCLOADDITION OF A VINYLIC OXIRANE FOLLOWED BY CLAISEN REARRANGEMENT CYCLOADDITION OF AN YNONE FOLLOWED BY NAZAROV CYCLIZATION CYCLOADDITION OF AN ACETOXYPYRANONE FOLLOWED BY CONJUGATE ADDITION CYCLOADDITION CASCADE INVOLVING ª-PYRANONE AND QUINONE SYSTEMS DOMINO TRANSFORMATIONS INVOLVING AN ELECTROCYCLIZATION REACTION METAL-MEDIATED CROSS COUPLING FOLLOWED BY ELECTROCYCLIZATION PALLADIUM-MEDIATED CROSS COUPLING/ELECTROCYCLIZATION REACTIONS CROSS COUPLING/6-ELECTROCYCLIZATION CROSS COUPLING/8-ELECTROCYCLIZATION CROSS COUPLING/8-ELECTROCYCLIZATION/6-ELECTROCYCLIZATION COPPER-CATALYZED TANDEM REACTIONS ZINC-CATALYZED TANDEM REACTIONS RUTHENIUM-CATALYZED FORMAL [2+2+2] CYCLOADDITION REACTIONS ALKYNE TRANSFORMATION FOLLOWED BY ELECTROCYCLIZATION ISOMERIZATION FOLLOWED BY ELECTROCYCLIZATION 1,3-HYDROGEN SHIFT/ELECTROCYCLIZATION 1,5-HYDROGEN SHIFT/ELECTROCYCLIZATION 1,7-HYDROGEN SHIFT/ELECTROCYCLIZATION CONSECUTIVE ELECTROCYCLIZATION REACTION CASCADES ALKENATION FOLLOWED BY ELECTROCYCLIZATION ELECTROCYCLIZATION FOLLOWED BY CYCLOADDITION MISCELLANEOUS REACTIONS ELECTROCYCLIZATION/OXIDATION PHOTOCHEMICAL ELIMINATION/ELECTROCYCLIZATION DOMINO RETRO-ELECTROCYCLIZATION REACTIONS HETERO-ELECTROCYCLIZATION AZA-ELECTROCYCLIZATION METAL-MEDIATED REACTION/HETERO-ELECTROCYCLIZATION IMINE OR IMINIUM FORMATION/HETERO-ELECTROCYCLIZATION ISOMERIZATION OR REARRANGEMENT/HETERO-ELECTROCYCLIZATION OXA-ELECTROCYCLIZATION THIA-ELECTROCYCLIZATION SIGMATROPIC SHIFTS AND ENE REACTIONS (EXCLUDING [3,3]) PRACTICAL CONSIDERATIONS DOMINO PROCESSES INITIATED BY ENE REACTIONS DOMINO PROCESSES INITIATED BY [2,3]-SIGMATROPIC REARRANGEMENTS DOMINO PROCESSES INITIATED BY OTHER SIGMATROPIC REARRANGEMENTS DOMINO PROCESSES IN THE SYNTHESIS OF NATURAL PRODUCTS DOMINO TRANSFORMATIONS INITIATED BY OR PROCEEDING THROUGH [3,3]-SIGMATROPIC REARRANGEMENTS COPE REARRANGEMENT FOLLOWED BY ENOLATE FUNCTIONALIZATION ANIONIC OXY-COPE REARRANGEMENT FOLLOWED BY INTERMOLECULAR ENOLATE ALKYLATION WITH ALKYL HALIDES ANIONIC OXY-COPE REARRANGEMENT FOLLOWED BY ENOLATE ALKYLATION BY PENDANT ALLYLIC ETHERS ANIONIC OXY-COPE REARRANGEMENT FOLLOWED BY ENOLATE ACYLATION AZA- AND OXONIA-COPE-CONTAINING DOMINO SEQUENCES IONIZATION-TRIGGERED OXONIA-COPE REARRANGEMENT FOLLOWED BY INTRAMOLECULAR NUCLEOPHILIC TRAPPING BY AN ENOL SILYL ETHER INTERMOLECULAR 1,4-ADDITION-TRIGGERED OXONIA-COPE REARRANGEMENT FOLLOWED BY INTRAMOLECULAR NUCLEOPHILIC TRAPPING BY A NASCENT ENOLATE IMINIUM-ION-FORMATION-TRIGGERED AZONIA-COPE REARRANGEMENT FOLLOWED BY INTRAMOLECULAR NUCLEOPHILIC TRAPPING BY A NASCENT ENAMINE DOUBLE, TANDEM HETERO-COPE REARRANGEMENT PROCESSES DOUBLE, TANDEM [3,3]-SIGMATROPIC REARRANGEMENT OF ALLYLIC, HOMOALLYLIC BIS(TRICHLOROACETIMIDATES) NEUTRAL CLAISEN REARRANGEMENT FOLLOWED BY FURTHER (NON-CLAISEN) PROCESSES OXY-COPE REARRANGEMENT/ENE REACTION DOMINO SEQUENCES OXY-COPE REARRANGEMENT/ENE REACTION/CLAISEN REARRANGEMENT AND OXY-COPE REARRANGEMENT/CLAISEN REARRANGEMENT/ENE REACTION DOMINO SEQUENCES CLAISEN REARRANGEMENT FOLLOWED BY ANOTHER PERICYCLIC PROCESS DOUBLE, TANDEM BELLUS–CLAISEN REARRANGEMENT REACTIONS CLAISEN REARRANGEMENT FOLLOWED BY [2,3]-SIGMATROPIC REARRANGEMENT CLAISEN REARRANGEMENT/DIELS–ALDER CYCLOADDITION DOMINO SEQUENCES CLAISEN REARRANGEMENT/[1,5]-H-SHIFT/6-ELECTROCYCLIZATION DOMINO SEQUENCES CLAISEN REARRANGEMENT FOLLOWED BY MULTIPLE PROCESSES PROPARGYL CLAISEN REARRANGEMENT FOLLOWED BY TAUTOMERIZATION, ACYLKETENE GENERATION, 6-ELECTROCYCLIZATION, AND AROMATIZATION PROPARGYL CLAISEN REARRANGEMENT FOLLOWED BY IMINE FORMATION, TAUTOMERIZATION, AND 6-ELECTROCYCLIZATION INTERMOLECULAR ALKYLATIVE DEAROMATIZATIONS OF PHENOLIC DERIVATIVES IN ORGANIC SYNTHESIS METAL-MEDIATED INTERMOLECULAR ALKYLATIVE DEAROMATIZATION OSMIUM(II)-MEDIATED INTERMOLECULAR ALKYLATIVE DEAROMATIZATION PALLADIUM-CATALYZED INTERMOLECULAR ALKYLATIVE DEAROMATIZATION TANDEM PALLADIUM-CATALYZED INTERMOLECULAR ALKYLATIVE DEAROMATIZATION/ANNULATION NON-METAL-MEDIATED INTERMOLECULAR ALKYLATIVE DEAROMATIZATION ALKYLATIVE DEAROMATIZATIONS OF PHENOLIC DERIVATIVES WITH ACTIVATED ELECTROPHILES ALKYLATIVE DEAROMATIZATIONS OF PHENOLIC DERIVATIVES WITH UNACTIVATED ELECTROPHILES TANDEM INTERMOLECULAR ALKYLATIVE DEAROMATIZATION/ANNULATION TANDEM ALKYLATIVE DEAROMATIZATION/[4+2] CYCLOADDITION TANDEM ALKYLATIVE DEAROMATIZATION/HYDROGENATION FOLLOWED BY LEWIS ACID CATALYZED CYCLIZATION TANDEM ALKYLATIVE DEAROMATIZATION/ANNULATION TO ACCESS TYPE A AND B POLYPRENYLATED ACYLPHLOROGLUCINOL DERIVATIVES ENANTIOSELECTIVE, TANDEM ALKYLATIVE DEAROMATIZATION/ANNULATION TANDEM ALKYLATIVE DEAROMATIZATION/RADICAL CYCLIZATION RECENT METHODS FOR ALKYLATIVE DEAROMATIZATION OF PHENOLIC DERIVATIVES RECENT APPLICATIONS TO INTERMOLECULAR ALKYLATIVE DEAROMATIZATION OF NAPHTHOLS DEAROMATIZATION REACTIONS AS DOMINO TRANSFORMATIONS TO ACCESS TYPE A AND B POLYPRENYLATED ACYLPHLOROGLUCINOL ANALOGUES ADDITIONS TO NONACTIVATED C=C BONDS DOMINO AMINATION PROTON-INITIATED EVENTS TRANSITION-METAL-INITIATED EVENTS HALOGEN-INITIATED EVENTS DOMINO ETHERIFICATION DOMINO CARBONYLATION DOMINO POLYENE CYCLIZATION CHALCOGEN-INITIATED EVENTS ORGANOCATALYZED ADDITION TO ACTIVATED C=C BONDS ORGANOCATALYZED DOMINO REACTIONS WITH ACTIVATED ALKENES: THE FIRST EXAMPLES PROLINOL TRIMETHYLSILYL ETHERS AS PRIVILEGED CATALYSTS FOR ENAMINE AND IMINIUM ION ACTIVATION INCREASING COMPLEXITY IN ORGANOCATALYZED DOMINO REACTIONS DOMINO ORGANOCATALYZED REACTIONS OF OXINDOLE DERIVATIVES FROM ENDERS DOMINO REACTIONS TO MELCHIORRES METHYLENE OXINDOLE MICHAEL ADDITION TO OXINDOLES SYNTHESIS OF TAMIFLU: THE HAYASHI APPROACH ONE-POT SYNTHESIS OF ABT-341, A DPP4-SELECTIVE INHIBITOR LARGE-SCALE INDUSTRIAL APPLICATION OF ORGANOCATALYTIC DOMINO REACTIONS: A CASE STUDY TRANSFERRING ORGANOCATALYTIC REACTIONS FROM ACADEMIA TO INDUSTRY: NOT STRAIGHTFORWARD THE REACTION DEVELOPED IN THE ACADEMIC ENVIRONMENT THE REACTION DEVELOPED IN THE INDUSTRIAL ENVIRONMENT ADDITION TO MONOFUNCTIONAL C=O BONDS TRANSITION-METAL-CATALYZED DOMINO ADDITION TO C=O BONDS DOMINO REACTIONS INVOLVING CARBONYL YLIDES REDUCTIVE ALDOL REACTIONS MICHAEL/ALDOL REACTIONS OTHER DOMINO ADDITION REACTIONS ORGANOCATALYTIC DOMINO ADDITION TO C=O BONDS AMINE-CATALYZED DOMINO ADDITION TO C=O BONDS ENAMINE-CATALYZED ALDOL/ALDOL REACTIONS ENAMINE-CATALYZED ALDOL/MICHAEL REACTIONS ENAMINE-CATALYZED DIELS–ALDER REACTIONS ENAMINE-CATALYZED MICHAEL/HENRY REACTIONS ENAMINE-CATALYZED MICHAEL/ALDOL REACTIONS ENAMINE-CATALYZED MICHAEL/HEMIACETALIZATION REACTIONS IMINIUM-CATALYZED MICHAEL/ALDOL REACTIONS IMINIUM-CATALYZED MICHAEL/HENRY REACTIONS IMINIUM-CATALYZED MICHAEL/MORITA–BAYLIS–HILLMAN REACTIONS IMINIUM-CATALYZED MICHAEL/HEMIACETALIZATION REACTIONS THIOUREA-CATALYZED DOMINO ADDITION TO C=O BONDS ALDOL/CYCLIZATION REACTIONS MICHAEL/HENRY REACTIONS MICHAEL/HEMIACETALIZATION REACTIONS PHOSPHORIC ACID CATALYZED DOMINO ADDITION TO C=O BONDS LEWIS ACID CATALYZED DOMINO ADDITION TO C=O BONDS ADDITIONS TO C=N BONDS AND NITRILES ADDITION TO C=N BONDS AND THE PICTET–SPENGLER STRATEGY UGI FIVE-CENTER FOUR-COMPONENT REACTION FOLLOWED BY POSTCONDENSATIONS ADDITION TO NITRILES