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Conversions of 9-chloro-4-azafluorene to azalenes

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The iodomethylate of 9-chloro-4-azafluorene is converted to 1H-1-methyl-indeno[1,2-b]pyridine when treated with base. We discuss the structure of compounds containing azalene fragments, which are formed upon heating 9-chloro-4-azafluorene. We discuss some considerations concerning the nomenclature of azulenes with the azafluorene skeleton.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 915–920, July 1992.

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Prostakov, N.S., Kruglyak, E.V., Shalimov, V.P. et al. Conversions of 9-chloro-4-azafluorene to azalenes. Chem Heterocycl Compd 28, 761–765 (1992). https://doi.org/10.1007/BF00474488

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  • DOI: https://doi.org/10.1007/BF00474488

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