Reaction of Amidine Phenylogous with p-Benzoquinones

DOI: 10.1246/bcsj.64.1966

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1966 - 1970 (1991)

Update date:2022-08-04

Topics: Column chromatography Thin-layer chromatography (TLC) Nucleophile Electrophile Synthetic route Recrystallization Mass spectrometry (MS) Nucleophilic addition Michael addition Aromaticity Reaction Monitoring Tautomerization Stoichiometry Solvent Evaporation Reaction yield redox reaction NMR spectroscopy (Nuclear Magnetic Resonance) p-Benzoquinones Conjugated system

Authors:

El-Din, Ahmed M. Nour

Mourad, Aboul-Fetouh E.

Hassan, Alaa A.

Gomaa, Mohsen A.

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Article abstract of DOI:10.1246/bcsj.64.1966

N-(4-Dimethylaminobenzylidene)anilines and N¹-(4-dimethylaminophenyl)-N¹,N²-diphenylformamidine reacted with tetrachloro-, tetrabromo-, and tetrafluoro-p-benzoquinones via charge-transfer complexes formation giving 2-monoa

Full text of DOI:10.1246/bcsj.64.1966

Products guided by the article

Product name:2,5-Dibromo-3,6-bis-(3-methoxy-phenylamino)-[1,4]benzoquinone

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