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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
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author Manna, Srimanta
Antonchick, Andrey P.
author_facet Manna, Srimanta
Antonchick, Andrey P.
author_sort Manna, Srimanta
collection PubMed
description 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.
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spelling pubmed-50716602016-11-02 [1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes Manna, Srimanta Antonchick, Andrey P. Angew Chem Int Ed Engl Communications 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. John Wiley and Sons Inc. 2016-03-21 2016-04-18 /pmc/articles/PMC5071660/ /pubmed/26997466 http://dx.doi.org/10.1002/anie.201600807 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Communications
Manna, Srimanta
Antonchick, Andrey P.
[1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes
title [1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes
title_full [1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes
title_fullStr [1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes
title_full_unstemmed [1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes
title_short [1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes
title_sort [1+1+1] cyclotrimerization for the synthesis of cyclopropanes
topic Communications
url 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
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