August 17, 2025French-Ukrainian Journal of ChemistryOpen Access

Beckmann Fragmentation of Camphor-4-carboxylic and Camphor-4-acetic Acid Oximes

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Authors

MGMarian V. Gorichko

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Implication

The recyclization reaction yields functionalized bicyclic lactones in nearly quantitative yields, suggesting broad applications for terpenoid synthesis.

Key Points

Beckmann fragmentation achieved nearly quantitative yields of functionalized bicyclic lactones.
The reaction produced lactones from camphor derivatives using aqueous hydrochloric acid in a mild environment.
This method allows for the large-scale synthesis of complex functionalized terpenoids from simple oximes.
The work highlights the efficiency and practicality of the recyclization reaction in organic synthesis.

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Marian V. Gorichko (2025) studied this question.

synapsesocial.com/papers/68c236b2b210217d647754ee https://doi.org/10.17721/fujcv13i1p104-109

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Implication

The recyclization reaction yields functionalized bicyclic lactones in nearly quantitative yields, suggesting broad applications for terpenoid synthesis.

Beckmann Fragmentation of Camphor-4-carboxylic and Camphor-4-acetic Acid Oximes

Discussion

Member takes

Implication

Key Points

Cite This Study

Beckmann Fragmentation of Camphor-4-carboxylic and Camphor-4-acetic Acid Oximes

Discussion

Member takes

Implication

Key Points

Cite This Study

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