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Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions

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Russian Chemical Bulletin Aims and scope

Abstract

The review considers the main results of the cycloaddition reactions involving cyclopropenes and methylenecyclopropanes, the compounds bearing strained three-membered rings and, respectively, endo- and exocyclic double bonds. The main attention is focused on the reactions of these compounds with 1,3-dipoles (nitrones, azomethine imines, azomethine ylides, carbonyl ylides, etc.), which gave complex heterocyclic systems with high regio- and stereoselectivity.

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Authors and Affiliations

  1. Institute of Chemistry, St. Petersburg State University, 26 Universitetskii prosp., 198504, St. Petersburg, Russian Federation

    A. P. Molchanov, M. M. Efremova & M. A. Kuznetsov

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  1. A. P. Molchanov
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  2. M. M. Efremova
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  3. M. A. Kuznetsov
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Correspondence to A. P. Molchanov or M. M. Efremova.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 620–650, April, 2022.

This work was financially supported by the Russian Foundation for Basic Research (Competition “Expansiya” No. 20-13-5014420).

No human or animal subjects were used in this research.

The authors declare no competing interests.

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Molchanov, A.P., Efremova, M.M. & Kuznetsov, M.A. Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions. Russ Chem Bull 71, 620–650 (2022). https://doi.org/10.1007/s11172-022-3460-z

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