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Continuous‐Flow Synthesis and Derivatization of Aziridines through Palladium‐Catalyzed C(sp(3))−H Activation
A continuous‐flow synthesis of aziridines by palladium‐catalyzed C(sp(3))−H activation is described. The new flow reaction could be combined with an aziridine‐ring‐opening reaction to give highly functionalized aliphatic amines through a consecutive process. A predictive mechanistic model was develo...
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/PMC5094502/ https://www.ncbi.nlm.nih.gov/pubmed/27304395 http://dx.doi.org/10.1002/anie.201602483 |
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author | Zakrzewski, Jacek Smalley, Adam P. Kabeshov, Mikhail A. Gaunt, Matthew J. Lapkin, Alexei A. |
author_facet | Zakrzewski, Jacek Smalley, Adam P. Kabeshov, Mikhail A. Gaunt, Matthew J. Lapkin, Alexei A. |
author_sort | Zakrzewski, Jacek |
collection | PubMed |
description | A continuous‐flow synthesis of aziridines by palladium‐catalyzed C(sp(3))−H activation is described. The new flow reaction could be combined with an aziridine‐ring‐opening reaction to give highly functionalized aliphatic amines through a consecutive process. A predictive mechanistic model was developed and used to design the C−H activation flow process and illustrates an approach towards first‐principles design based on novel catalytic reactions. |
format | Online Article Text |
id | pubmed-5094502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50945022016-11-09 Continuous‐Flow Synthesis and Derivatization of Aziridines through Palladium‐Catalyzed C(sp(3))−H Activation Zakrzewski, Jacek Smalley, Adam P. Kabeshov, Mikhail A. Gaunt, Matthew J. Lapkin, Alexei A. Angew Chem Int Ed Engl Communications A continuous‐flow synthesis of aziridines by palladium‐catalyzed C(sp(3))−H activation is described. The new flow reaction could be combined with an aziridine‐ring‐opening reaction to give highly functionalized aliphatic amines through a consecutive process. A predictive mechanistic model was developed and used to design the C−H activation flow process and illustrates an approach towards first‐principles design based on novel catalytic reactions. John Wiley and Sons Inc. 2016-06-15 2016-07-25 /pmc/articles/PMC5094502/ /pubmed/27304395 http://dx.doi.org/10.1002/anie.201602483 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 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Zakrzewski, Jacek Smalley, Adam P. Kabeshov, Mikhail A. Gaunt, Matthew J. Lapkin, Alexei A. Continuous‐Flow Synthesis and Derivatization of Aziridines through Palladium‐Catalyzed C(sp(3))−H Activation |
title | Continuous‐Flow Synthesis and Derivatization of Aziridines through Palladium‐Catalyzed C(sp(3))−H Activation |
title_full | Continuous‐Flow Synthesis and Derivatization of Aziridines through Palladium‐Catalyzed C(sp(3))−H Activation |
title_fullStr | Continuous‐Flow Synthesis and Derivatization of Aziridines through Palladium‐Catalyzed C(sp(3))−H Activation |
title_full_unstemmed | Continuous‐Flow Synthesis and Derivatization of Aziridines through Palladium‐Catalyzed C(sp(3))−H Activation |
title_short | Continuous‐Flow Synthesis and Derivatization of Aziridines through Palladium‐Catalyzed C(sp(3))−H Activation |
title_sort | continuous‐flow synthesis and derivatization of aziridines through palladium‐catalyzed c(sp(3))−h activation |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094502/ https://www.ncbi.nlm.nih.gov/pubmed/27304395 http://dx.doi.org/10.1002/anie.201602483 |
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