Angew. Chem. Int. Ed. Engl.

1984

DOI: 10.1002/anie.198406221

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1,4,7,10‐Tetraphenyldibenzo[a,e]cyclooctene‐5,6,11,12‐tetrone from 3,6‐Diphenylphthalic Anhydride

¹

,

Georg W. Ollmann

²

,

³

Abstract: Durch kathodische Reduktion des Anhydrids (I) werden die Dimeren (II) und (III) erhalten.

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Cited by 6 publications

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Elektroreduktion organischer Verbindungen. 22. Darstellung aromatischer Aldehyde durch Elektroreduktion von Estern und Amiden in Gegenwart von Chlortrimethylsilan

Goetz‐Schatowitz

¹

,

²

,

³

et al. 1993

J. Prakt. Chem.

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Electrochemical Reduction of Organic Compounds. 22. Preparation of Aromatic Aldehydes by Electroreduction of Esters and Amides in the Presence of Chlorotrimethylsilane The electroreduction of aromatic esters 1 and amides 9 in dry acetonitrile in the presence of chlorotrimethylsilane 2 affords aldehydes 3 in moderate to good yields depending on the aromatic substituents. The formation of 3 and characteristic by‐products is discussed.

Elektroreduktion organischer Verbindungen. 22. Darstellung aromatischer Aldehyde durch Elektroreduktion von Estern und Amiden in Gegenwart von Chlortrimethylsilan

Goetz‐Schatowitz

¹

,

²

,

³

et al. 1993

J. Prakt. Chem.

View full text Add to dashboard Cite

Electrochemical Reduction of Organic Compounds. 22. Preparation of Aromatic Aldehydes by Electroreduction of Esters and Amides in the Presence of Chlorotrimethylsilane The electroreduction of aromatic esters 1 and amides 9 in dry acetonitrile in the presence of chlorotrimethylsilane 2 affords aldehydes 3 in moderate to good yields depending on the aromatic substituents. The formation of 3 and characteristic by‐products is discussed.

Electrochemistry of organic acceptor compounds: aromatic anhydrides

Luca¹,

1987

Journal of Electroanalytical Chemistry and Interfacial Electroc

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No abstract

Furans and their Benzo Derivatives: Synthesis

¹

1996

Comprehensive Heterocyclic Chemistry II

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No abstract

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