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[1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes

The synthesis of small rings by functionalization of C(sp(3))−H bonds remains a great challenge. We report for the first time a copper‐catalyzed [1+1+1] cyclotrimerization of acetophenone derivatives under mild reaction conditions. The reaction has a broad scope for the stereoselective synthesis of...

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Detalles Bibliográficos
Autores principales: Manna, Srimanta, Antonchick, Andrey P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071660/
https://www.ncbi.nlm.nih.gov/pubmed/26997466
http://dx.doi.org/10.1002/anie.201600807
Descripción
Sumario:The synthesis of small rings by functionalization of C(sp(3))−H bonds remains a great challenge. We report for the first time a copper‐catalyzed [1+1+1] cyclotrimerization of acetophenone derivatives under mild reaction conditions. The reaction has a broad scope for the stereoselective synthesis of cyclopropanes by trimerization of acetophenone. The developed transformation is based on an extraordinary copper‐catalyzed cascade process that allows saturated carbocycles to be obtained for the first time by cyclotrimerization through functionalization of C(sp(3))−H bonds. The cascade of sixfold C(sp(3))−H bond functionalization allows the synthesis of cyclopropanes in a highly stereoselective approach.