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Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tricyclic aziridines. These undergo a range of novel palladium-catalyzed ring-opening and cycloaddition reactions, likely driven by their inherent strain, allowing incorporation of further functionality...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977501/ https://www.ncbi.nlm.nih.gov/pubmed/29910920 http://dx.doi.org/10.1039/c5sc04062k |
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author | Blackham, Emma E. Knowles, Jonathan P. Burgess, Jonathan Booker-Milburn, Kevin I. |
author_facet | Blackham, Emma E. Knowles, Jonathan P. Burgess, Jonathan Booker-Milburn, Kevin I. |
author_sort | Blackham, Emma E. |
collection | PubMed |
description | Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tricyclic aziridines. These undergo a range of novel palladium-catalyzed ring-opening and cycloaddition reactions, likely driven by their inherent strain, allowing incorporation of further functionality by fusing additional heterocyclic rings onto these already complex polycyclic cores. This rapid, 2-step access to complex sp(3) – rich heterocycles should be of interest to those in the fields of drug discovery and natural product synthesis. |
format | Online Article Text |
id | pubmed-5977501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-59775012018-06-15 Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles Blackham, Emma E. Knowles, Jonathan P. Burgess, Jonathan Booker-Milburn, Kevin I. Chem Sci Chemistry Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tricyclic aziridines. These undergo a range of novel palladium-catalyzed ring-opening and cycloaddition reactions, likely driven by their inherent strain, allowing incorporation of further functionality by fusing additional heterocyclic rings onto these already complex polycyclic cores. This rapid, 2-step access to complex sp(3) – rich heterocycles should be of interest to those in the fields of drug discovery and natural product synthesis. Royal Society of Chemistry 2016-03-01 2016-01-04 /pmc/articles/PMC5977501/ /pubmed/29910920 http://dx.doi.org/10.1039/c5sc04062k Text en This journal is © The Royal Society of Chemistry 2016 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 Blackham, Emma E. Knowles, Jonathan P. Burgess, Jonathan Booker-Milburn, Kevin I. Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles |
title | Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
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title_full | Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
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title_fullStr | Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
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title_full_unstemmed | Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
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title_short | Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
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title_sort | combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977501/ https://www.ncbi.nlm.nih.gov/pubmed/29910920 http://dx.doi.org/10.1039/c5sc04062k |
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