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[1,7]-Electrocyclization reactions in the synthesis of azepine derivatives

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Chemistry of Heterocyclic Compounds Aims and scope

The review is devoted to the synthesis of azepine structures by [1,7]-electrocyclization reactions of unsaturated azomethine ylides and azatriene anions.

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The authors thank the Russian Foundation for Basic Research for financial support (grant 09-03-00890a).

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  1. A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St., Irkutsk, 664033, Russia

    N. A. Nedolya & B. A. Trofimov

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 166–190, January, 2013.

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Nedolya, N.A., Trofimov, B.A. [1,7]-Electrocyclization reactions in the synthesis of azepine derivatives. Chem Heterocycl Comp 49, 152–176 (2013). https://doi.org/10.1007/s10593-013-1236-y

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