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1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes

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Chemistry of Heterocyclic Compounds Aims and scope

In this review, we consider 1,3-dipolar cycloaddition reactions between azomethine ylides and alkynes, resulting in the formation of pyrroles, as well as their hydrogenated and fused analogs. The references have been arranged according to the types of azomethine ylides and the methods used for their generation. The review is mainly focused on literature sources published since year 2000 and contains 133 references.

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Notes

  1. Active lead was obtained by reducing lead acetate with sodium borohydride in aqueous acetic acid.

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Acknowledgment

This work was performed with financial support from the Southern Federal University (internal grant BnGr-

07/2017-18).

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  1. Faculty of Chemistry, Southern Federal University, 7 Zorge St, Rostov-on-Don, 344090, Russia

    Anna V. Gulevskaya & Julia I. Nelina-Nemtseva

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  1. Anna V. Gulevskaya
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  2. Julia I. Nelina-Nemtseva
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Correspondence to Anna V. Gulevskaya.

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Dedicated to Professor A. F. Pozharskii on his 80th birthday

Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2018, 54(12), 1084–1107

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Gulevskaya, A.V., Nelina-Nemtseva, J.I. 1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes. Chem Heterocycl Comp 54, 1084–1107 (2018). https://doi.org/10.1007/s10593-019-02398-5

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