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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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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. |
format | Online Article Text |
id | pubmed-5071660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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