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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...

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Autores principales: Xu, Xue, Wang, Yong, Cui, Xin, Wojtas, Lukasz, Zhang, X. Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
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.
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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
title_full Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
title_fullStr Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
title_full_unstemmed Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
title_short Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes
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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