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   <subfield code="a">Zur Synthese und Struktur der p -Indazolchinone und ihrer Methylierungsprodukte Untersuchungen über Chinone, 8. Mitt</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Robert Ott, Erfried Pinter]</subfield>
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   <subfield code="a">Synthesis and structure of p -indazolquinones and their methylation products. Studies on quinones, VIII</subfield>
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   <subfield code="a">Summary: Thep-benzoquinones5e-j react with diazomethane (after dehydrogenation) to 6-anilino-2e, dimethylamino-2h, phenylthio-2i, and methylthioindazolquinone2j. Methylation with dimethylsulfate of these as well as of the already known indazolquinones 6-toluidino-2f, 6-methylanilino-2g, 5-tert.butyl-2m, 5,6-methyl- (isomer mixture)2l,n, and benz-indazolquinone2o yield the 1-and 2-N-methyl derivatives3 and4. The structure of the 2-methyl derivatives is established by reaction of the corresponding benzoquinones with 3-methylsydnon in the case of4e,4g. UV/VIS-, IR- and1H-NMR-spectroscopy (in CDCl3 andDMSO) were used for structure determination. Comparison of the UV/VIS-spectra of2-4 shows that the indazolquinones are existing as 2 H-4,7-diones. For the structure elucidation of the 1- rs. 2-methylderivatives (whichh can be attributed to the methylation products) NMR-spectroscopy is well suited even without knowing the second isomer (solvent-effect). The course of the reaction of quinones with diazomethane and of the methylation reactions of the indazolquinones is discussed.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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