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Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions

The bis(imino)pyridine iron complex, for the first time, is developed as an effective metal carbene catalyst for carbene transfer reactions of donor–acceptor diazo compounds. Its broad catalytic capability is demonstrated by a range of metal carbene reactions, from cyclopropanation, cyclopropenation...

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Detalles Bibliográficos
Autores principales: Wang, Ban, Howard, Isaac G., Pope, Jackson W., Conte, Eric D., Deng, Yongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839806/
https://www.ncbi.nlm.nih.gov/pubmed/31853351
http://dx.doi.org/10.1039/c9sc02189b
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author Wang, Ban
Howard, Isaac G.
Pope, Jackson W.
Conte, Eric D.
Deng, Yongming
author_facet Wang, Ban
Howard, Isaac G.
Pope, Jackson W.
Conte, Eric D.
Deng, Yongming
author_sort Wang, Ban
collection PubMed
description The bis(imino)pyridine iron complex, for the first time, is developed as an effective metal carbene catalyst for carbene transfer reactions of donor–acceptor diazo compounds. Its broad catalytic capability is demonstrated by a range of metal carbene reactions, from cyclopropanation, cyclopropenation, epoxidation, and Doyle–Kirmse reaction to O–H insertion, N–H insertion, and C–H insertion reactions. The asymmetric cyclopropanation of styrene and methyl phenyldiazoacetate was successfully achieved by the new chiral bis(imino)pyridine iron catalyst, which delivers a new gateway for the development of chiral iron catalysis for metal carbene reactions.
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spelling pubmed-68398062019-12-18 Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions Wang, Ban Howard, Isaac G. Pope, Jackson W. Conte, Eric D. Deng, Yongming Chem Sci Chemistry The bis(imino)pyridine iron complex, for the first time, is developed as an effective metal carbene catalyst for carbene transfer reactions of donor–acceptor diazo compounds. Its broad catalytic capability is demonstrated by a range of metal carbene reactions, from cyclopropanation, cyclopropenation, epoxidation, and Doyle–Kirmse reaction to O–H insertion, N–H insertion, and C–H insertion reactions. The asymmetric cyclopropanation of styrene and methyl phenyldiazoacetate was successfully achieved by the new chiral bis(imino)pyridine iron catalyst, which delivers a new gateway for the development of chiral iron catalysis for metal carbene reactions. Royal Society of Chemistry 2019-07-02 /pmc/articles/PMC6839806/ /pubmed/31853351 http://dx.doi.org/10.1039/c9sc02189b Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Wang, Ban
Howard, Isaac G.
Pope, Jackson W.
Conte, Eric D.
Deng, Yongming
Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions
title Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions
title_full Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions
title_fullStr Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions
title_full_unstemmed Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions
title_short Bis(imino)pyridine iron complexes for catalytic carbene transfer reactions
title_sort bis(imino)pyridine iron complexes for catalytic carbene transfer reactions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839806/
https://www.ncbi.nlm.nih.gov/pubmed/31853351
http://dx.doi.org/10.1039/c9sc02189b
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