Fe III ‐Mediated Synthesis of Azaspirodienones via Ipso ‐Radical Cyclization of Ugi–4CR Adducts

A concise and operationally simple two‐step protocol for the efficient synthesis of azaspirodienones through Fe III ‐mediated ipso ‐radical cyclization of Ugi adducts has been developed. The strategy combines the versatility of multicomponent Ugi reactions with the synthetic power of radical cyclization, enabling rapid construction of structurally complex and medicinally relevant spirocyclic frameworks from readily accessible starting materials.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-09-11
DOI
https://doi.org/10.1002/ejoc.70846
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00

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article

Fe III ‐Mediated Synthesis of Azaspirodienones via Ipso ‐Radical Cyclization of Ugi–4CR Adducts

Luis A. Polindara‐García, Silvia J. Becerra‐Anaya, Valeria Morales–Hernández
European Journal of Organic Chemistry
Multicomponent Synthesis of Heterocycles
article

Fe III ‐Mediated Synthesis of Azaspirodienones via Ipso ‐Radical Cyclization of Ugi–4CR Adducts

Luis A. Polindara‐García, Silvia J. Becerra‐Anaya, Valeria Morales–Hernández
article en

Abstract

A concise and operationally simple two‐step protocol for the efficient synthesis of azaspirodienones through Fe III ‐mediated ipso ‐radical cyclization of Ugi adducts has been developed. The strategy combines the versatility of multicomponent Ugi reactions with the synthetic power of radical cyclization, enabling rapid construction of structurally complex and medicinally relevant spirocyclic frameworks from readily accessible starting materials.

European Journal of Organic Chemistry
Universidad Nacional Autónoma de México (MX)
Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México
Openalex Percentile: Top 21%
Multicomponent Synthesis of Heterocycles
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