Synthesis of o-Quinones of 3H-Benzindole

DOI: 10.1007/BF00505760

Source and publish data:

Chemistry of Heterocyclic Compounds p. 1086 - 1087 (1983)

Update date:2022-07-30

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Authors:

Grinev, A. N.

Sorokina, I. K.

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Article abstract of DOI:10.1007/BF00505760

4,5-Dioxo-4,5-dihydro-3H-benzindole derivatives were synthesized from 3-nitro-o-naphthoquinones with keto enol residues in the 4 position.One of these products was methylated at the nitrogen atom of the pyrrole ring.The N-methyl derivative was used for the synthesis of a phenazine.

Full text of DOI:10.1007/BF00505760

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Product name:3H-Benz[e]indole-1-carboxylic acid, 8-bromo-4,5-dihydro-4,5-dioxo-2-phenyl-, ethyl ester

Cas No:88418-60-4

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