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   <subfield code="a">Synthesis and structure of derivatives of azadithiapentaleneanthrone and isothiazoleanthrone</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[M. Gorelik, R. Alimova, V. Shteiman, T. Gladysheva, V. Tafeenko, S. Medvedev]</subfield>
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   <subfield code="a">The reaction of N,N′-dialkyl- or N,N′-diaryl-1,5-diaminoanthrones with sulfur in a polar aprotic solvent in the presence of a base leads to the formation of 4-alkyl(aryl)amino-9-alky(aryl)-5H-anthra[1,9,8-bcde]-9-aza-1,10λ4-di-thiapentalen-5-ones. The reaction of the 1,5-diaminoanthrone, followed by methylation, leads to 7-amino-10-methylthio- and 7-amino-8,10-dimethylthio-6H-anthra[9,1-cd]isothiazol-6-ones. The structures of the last two compounds and of 4-methylamino-9-methylazadithiapentaleneanthrone were studied by x-ray crystallography. Elimination of the amino group occurs in each series. The structural features and the spectral characteristics of the new heterocyclic systems are discussed.</subfield>
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   <subfield code="t">Chemistry of Heterocyclic Compounds</subfield>
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