Bisindoles. 38. Synthesis of Some Derivatives of 1H,6H-Indolo[7,6-g]indole |
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Authors: | Sh. A. Samsoniya M. V. Trapaidze N. N. Machaidze G. Dürr |
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Affiliation: | (1) Iv. Javakhishvili Tbilisi State University, Tbilisi, Georgia;(2) Saarland University, Saarbrücken, Germany |
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Abstract: | 1H,6H,2,3,7,8-Tetramethylindolo[7,6-g]indole and 1H,8H,2,3,4,5,9,10,11,12-octahydrocarbazolo[3,2-c]carbazole were synthesized by the condensation of 1,5-naphthylenedihydrazine with alkyl ketones followed by cyclization of the obtained hydrazones without isolation. The respective N,N-dibenzyl derivatives were obtained by benzylation of the alkyl-substituted compounds. A new spirocyclic system was synthesized by nucleophilic addition of 2,3,3,7,8,8-hexamethylindolenino[7,6-g]indolenine to 2',3'-dimethoxycarbonylspirofluorenecyclopropene. |
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Keywords: | indoloindole carbazolocarbazole spirocyclopropene photochrome benzylation indolization |
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