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Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
For the first time, α-formyldiazoacetates have been successfully applied for the asymmetric cyclopropanation of alkenes via Co(ii)-based metalloradical catalysis. The cobalt(ii) complex of the D (2)-symmetric chiral amidoporphyrin [Co(3,5-Di( t )Bu-ChenPhyrin)] is an effective metalloradical catalys...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605771/ https://www.ncbi.nlm.nih.gov/pubmed/28959396 http://dx.doi.org/10.1039/c7sc00658f |
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author | Xu, Xue Wang, Yong Cui, Xin Wojtas, Lukasz Zhang, X. Peter |
author_facet | Xu, Xue Wang, Yong Cui, Xin Wojtas, Lukasz Zhang, X. Peter |
author_sort | Xu, Xue |
collection | PubMed |
description | For the first time, α-formyldiazoacetates have been successfully applied for the asymmetric cyclopropanation of alkenes via Co(ii)-based metalloradical catalysis. The cobalt(ii) complex of the D (2)-symmetric chiral amidoporphyrin [Co(3,5-Di( t )Bu-ChenPhyrin)] is an effective metalloradical catalyst that can activate α-formyldiazoacetates to cyclopropanate both aromatic and aliphatic olefins with varied electronic properties, affording the synthetically useful 1,1-cyclopropaneformylesters in high yields with both high diastereo- and enantioselectivity. |
format | Online Article Text |
id | pubmed-5605771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-56057712017-09-28 Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes Xu, Xue Wang, Yong Cui, Xin Wojtas, Lukasz Zhang, X. Peter Chem Sci Chemistry For the first time, α-formyldiazoacetates have been successfully applied for the asymmetric cyclopropanation of alkenes via Co(ii)-based metalloradical catalysis. The cobalt(ii) complex of the D (2)-symmetric chiral amidoporphyrin [Co(3,5-Di( t )Bu-ChenPhyrin)] is an effective metalloradical catalyst that can activate α-formyldiazoacetates to cyclopropanate both aromatic and aliphatic olefins with varied electronic properties, affording the synthetically useful 1,1-cyclopropaneformylesters in high yields with both high diastereo- and enantioselectivity. Royal Society of Chemistry 2017-06-01 2017-03-31 /pmc/articles/PMC5605771/ /pubmed/28959396 http://dx.doi.org/10.1039/c7sc00658f Text en This journal is © The Royal Society of Chemistry 2017 https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Xu, Xue Wang, Yong Cui, Xin Wojtas, Lukasz Zhang, X. Peter Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes |
title | Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
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title_full | Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
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title_fullStr | Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
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title_full_unstemmed | Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
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title_short | Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
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title_sort | metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605771/ https://www.ncbi.nlm.nih.gov/pubmed/28959396 http://dx.doi.org/10.1039/c7sc00658f |
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