Ring Expansion Reactions via C-N Bond Cleavage in the Synthesis of Medium-sized Cycles and Macrocycles

Authors

DOI:

https://doi.org/10.24959/ophcj.24.312453

Keywords:

cleavage, ring expansion, aminal, amidines, medium-sized cycles, macrocycles

Abstract

The literature review discusses and systematizes synthetic approaches to medium-sized cycles and macrocycles based on ring expansion reactions of bi- or polycyclic systems via C-N bond cleavage. Ring expansion reactions of bicyclic ammonium salts proceed via thermal decomposition or the action of strong bases. Bi- or polycyclic systems containing a common amine group can be reduced with strong reducing reagents, e.g. lithium aluminum hydride. Ammonium derivatives are much more prone to nucleophilic attack and quite often are used as starting materials for the synthesis of medium-sized cycles. Bicyclic systems containing a common aminal or amidine group are used for the synthesis of medium-sized rings and macrocycles via cleavage of the endocyclic C-N bond. Various methods of their activation and reduction are discussed in the review.

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  • The authors received no specific funding for this work.

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Published

2024-11-08

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(1)
Lysenko, V.; Nazarenko, K.; Kostyuk, O. Ring Expansion Reactions via C-N Bond Cleavage in the Synthesis of Medium-Sized Cycles and Macrocycles. J. Org. Pharm. Chem. 2024, 22, 26-40.

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Vol. 22 No. 2 (2024)

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Review Articles

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