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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...

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Detalles Bibliográficos
Autores principales: Blackham, Emma E., Knowles, Jonathan P., Burgess, Jonathan, Booker-Milburn, Kevin I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
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.
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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
title_full Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
title_fullStr Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
title_full_unstemmed Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
title_short Combining photochemistry and catalysis: rapid access to sp(3) – rich polyheterocycles from simple pyrroles
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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