Article

On Quinone as Oxidising Agent in the Oppenauer-Oxidation

Authors:
To read the full-text of this research, you can request a copy directly from the authors.

No full-text available

Request Full-text Paper PDF

To read the full-text of this research,
you can request a copy directly from the authors.

Chapter
Abbau quartäre AmmoniumhydroxideAbbau quartäre AmmoniumsalzeAbspaltungs-RegelAcetessigester-ReduktionAcetessigester-SynthesenAcetylen-AdditionAllen-UmlagerungenAcinitroalkan-SpaltungAcridin-RingschlussAcridinring-KondensationAcridon-SyntheseAcridon-Syntheseα-Acylaminoketon-SyntheseAcylierunghydrierende AcylierungAromaten AcylierungC-AcylierungAcyllacton-UmlagerungAcyloin-Umlagerungnucleophile AdditionAdditionsregelAldehyd-AbfangreaktionAldehyd-AlkylierungAldehyd-DismutationAldehydAldehyd-NachweisAldehyd-OxidationAldehyd-SyntheseAldehyde aus NitronenAldimin-BildungAldol-AdditionAldol-KondensationAldonsäureamid-AbbauAldose-N-GlykosidAlkindiol-ReduktionAlkohol-DehydrierungAlkohol-SelbstkondensationAlkoholat-AlkylierungAlkylamin-AbbauN-AlkylanilinC-Alkylanilin-UmlagerungAlkylcarbenium-UmlagerungAlkylhalogenid-KondensationAlkylhalogenid-Oxidationalkylierender AbbauAlkylierungAlkylierungArylierungAlkylphosphonyldichlorid-DarstellungAlkylradikal-NachweisAlkylwanderungAlloxazin-RingschlussO-AllylC-Allyl-UmlagerungAllyl-BromierungAllylumlagerungAmid-RegelAmidomethylierungAmidoximAmin-AbbauAmin-AlkylierungAmin-BestimmungAmin-MethylierungAmin-SulfonierungAmin-SyntheseAminoalkylierungα-AminoalkylierungAminomethylierungAminobenzylierungAminosäure-ReduktionAminosäure-Syntheseo-Aminothiophenol-SyntheseAminoxidAmmoniak-Mathan-Oxidationanaerober Glucose-Abbauangulare MethylierungAnil-KondensationAnthracen-RingschlussAnthracen-SyntheseAnthrachinon-HydroxylierungAromatische Stabilitäts-RegelArsenit-ArylierungArsensäureschmelzeArsonylierungAryl-alkylether-SpaltungAryl-FormylierungAryl-HydrierungArylazid-DarstellungAryldiazoalkan-DarstellungArylhydrazon-DarstellungArylnitril-SyntheseArylwanderungAsymmetrie-InduktionsregelAzlacton-KondensationAldehyd-Rhodanin-KondensationAzlacton-SpaltungAzoxybenzol-UmlagerungAzulen-Synthese
Article
The paper describes the change of the author’s research from synthetic organic chemistry to electrochemistry and the advantages and disadvantages of having been trained in organic synthesis rather than in electrochemistry. The described research in electrochemistry includes, among other projects, oxidations in non-aqueous solvents, reduction of azomethine derivatives and heterocyclic compounds, synthesis of heterocyclic compounds, reduction of graphite, electrocatalytic reductions, electron transfer in nucleophilic substitutions and additions, determination of redox potentials of short-lived radicals, and electrochemical formation of Grignard compounds having reducible groups. At the end, some considerations after 60years of research are included. KeywordsOxidations–Azomethine compounds–Heterocycles–Electrocatalysis–Electron transfer–Potentials of radicals
ResearchGate has not been able to resolve any references for this publication.