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• W2000618880 abstract "The treatment of 3,3a,4,5‐tetrahydro‐3‐aryl‐2‐phenyl‐2 H ‐benzo[g]indazoles 4 with I 2 /DMSO led to the oxidation of the five‐member rings ( 5 ) as well as the iodination of N ‐phenyl moieties along with oxidation of the five‐member rings ( 6 ). However, the reactions of 4 with CuCl 2 /DMSO gave only compounds 5 . The reaction of N ‐bromosuccinimide (NBS) with compounds 4 resulted in fully aromatization along with bromination at C‐5 of the indazole rings ( 7 ). The indazole six‐member rings in compounds 5 and 6 also underwent aromatization along with bromination by using NBS ( 7 and 8 )." @default.
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• W2000618880 date "2012-11-01" @default.
• W2000618880 modified "2023-10-18" @default.
• W2000618880 title "Aromatization and Halogenation of 3,3a,4,5-Tetrahydro-3-aryl-2-phenyl-2<i>H</i>-benzo[g]indazole Using I₂/DMSO, CuCl₂/DMSO, and<i>N</i>-Bromosuccinimide" @default.
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• W2000618880 doi "https://doi.org/10.1002/jhet.1049" @default.
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