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Construction of Polycyclic γ-Lactams and Related Heterocycles via Electron Catalysis
[Image: see text] Cascade radical cyclization of 1,6-enynes for the construction of biologically important polycyclic γ-lactams and related heterocycles is reported. In these radical cascade processes, three new C–C bonds are formed and transition metals are not required to run these sequences. The...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168651/ https://www.ncbi.nlm.nih.gov/pubmed/27978670 http://dx.doi.org/10.1021/acs.orglett.6b03267 |
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author | Xuan, Jun Daniliuc, Constantin G. Studer, Armido |
author_facet | Xuan, Jun Daniliuc, Constantin G. Studer, Armido |
author_sort | Xuan, Jun |
collection | PubMed |
description | [Image: see text] Cascade radical cyclization of 1,6-enynes for the construction of biologically important polycyclic γ-lactams and related heterocycles is reported. In these radical cascade processes, three new C–C bonds are formed and transition metals are not required to run these sequences. The mild reaction conditions, broad substrate scope, and the importance of the heterocyclic products render the approach valuable. |
format | Online Article Text |
id | pubmed-5168651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-51686512016-12-21 Construction of Polycyclic γ-Lactams and Related Heterocycles via Electron Catalysis Xuan, Jun Daniliuc, Constantin G. Studer, Armido Org Lett [Image: see text] Cascade radical cyclization of 1,6-enynes for the construction of biologically important polycyclic γ-lactams and related heterocycles is reported. In these radical cascade processes, three new C–C bonds are formed and transition metals are not required to run these sequences. The mild reaction conditions, broad substrate scope, and the importance of the heterocyclic products render the approach valuable. American Chemical Society 2016-11-29 2016-12-16 /pmc/articles/PMC5168651/ /pubmed/27978670 http://dx.doi.org/10.1021/acs.orglett.6b03267 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Xuan, Jun Daniliuc, Constantin G. Studer, Armido Construction of Polycyclic γ-Lactams and Related Heterocycles via Electron Catalysis |
title | Construction of Polycyclic γ-Lactams
and Related Heterocycles via Electron Catalysis |
title_full | Construction of Polycyclic γ-Lactams
and Related Heterocycles via Electron Catalysis |
title_fullStr | Construction of Polycyclic γ-Lactams
and Related Heterocycles via Electron Catalysis |
title_full_unstemmed | Construction of Polycyclic γ-Lactams
and Related Heterocycles via Electron Catalysis |
title_short | Construction of Polycyclic γ-Lactams
and Related Heterocycles via Electron Catalysis |
title_sort | construction of polycyclic γ-lactams
and related heterocycles via electron catalysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5168651/ https://www.ncbi.nlm.nih.gov/pubmed/27978670 http://dx.doi.org/10.1021/acs.orglett.6b03267 |
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