Cargando…
A mild catalytic system for radical conjugate addition of nitrogen heterocycles
The direct addition of pyridine and diazine units to electron-poor alkenes has been achieved via a redox radical mechanism that is enabled by limiting the effective concentration of the hydrogen-atom source. The described method is tolerant of acidic functional groups and is generally applicable to...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412691/ https://www.ncbi.nlm.nih.gov/pubmed/28507687 http://dx.doi.org/10.1039/c7sc00243b |
_version_ | 1783233058210578432 |
---|---|
author | Aycock, R. A. Wang, H. Jui, N. T. |
author_facet | Aycock, R. A. Wang, H. Jui, N. T. |
author_sort | Aycock, R. A. |
collection | PubMed |
description | The direct addition of pyridine and diazine units to electron-poor alkenes has been achieved via a redox radical mechanism that is enabled by limiting the effective concentration of the hydrogen-atom source. The described method is tolerant of acidic functional groups and is generally applicable to the union of a wide range of Michael acceptors and 6-membered heterocyclic halides. |
format | Online Article Text |
id | pubmed-5412691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-54126912017-05-15 A mild catalytic system for radical conjugate addition of nitrogen heterocycles Aycock, R. A. Wang, H. Jui, N. T. Chem Sci Chemistry The direct addition of pyridine and diazine units to electron-poor alkenes has been achieved via a redox radical mechanism that is enabled by limiting the effective concentration of the hydrogen-atom source. The described method is tolerant of acidic functional groups and is generally applicable to the union of a wide range of Michael acceptors and 6-membered heterocyclic halides. Royal Society of Chemistry 2017-04-01 2017-02-13 /pmc/articles/PMC5412691/ /pubmed/28507687 http://dx.doi.org/10.1039/c7sc00243b Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Aycock, R. A. Wang, H. Jui, N. T. A mild catalytic system for radical conjugate addition of nitrogen heterocycles |
title | A mild catalytic system for radical conjugate addition of nitrogen heterocycles
|
title_full | A mild catalytic system for radical conjugate addition of nitrogen heterocycles
|
title_fullStr | A mild catalytic system for radical conjugate addition of nitrogen heterocycles
|
title_full_unstemmed | A mild catalytic system for radical conjugate addition of nitrogen heterocycles
|
title_short | A mild catalytic system for radical conjugate addition of nitrogen heterocycles
|
title_sort | mild catalytic system for radical conjugate addition of nitrogen heterocycles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412691/ https://www.ncbi.nlm.nih.gov/pubmed/28507687 http://dx.doi.org/10.1039/c7sc00243b |
work_keys_str_mv | AT aycockra amildcatalyticsystemforradicalconjugateadditionofnitrogenheterocycles AT wangh amildcatalyticsystemforradicalconjugateadditionofnitrogenheterocycles AT juint amildcatalyticsystemforradicalconjugateadditionofnitrogenheterocycles AT aycockra mildcatalyticsystemforradicalconjugateadditionofnitrogenheterocycles AT wangh mildcatalyticsystemforradicalconjugateadditionofnitrogenheterocycles AT juint mildcatalyticsystemforradicalconjugateadditionofnitrogenheterocycles |