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De Novo Synthesis of Multisubstituted Aryl Amines Using Alkene Cross Metathesis
[Image: see text] The olefin cross-metathesis reaction allows rapid access to 1,5-dicarbonyl intermediates which, upon treatment with a primary or secondary amine, allow the synthesis of a range of multisubstituted carbocyclic aryl amines. This de novo arene synthesis yields nonclassical substitutio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979090/ https://www.ncbi.nlm.nih.gov/pubmed/24646289 http://dx.doi.org/10.1021/ol500441q |
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author | Tatton, Matthew R. Simpson, Iain Donohoe, Timothy J. |
author_facet | Tatton, Matthew R. Simpson, Iain Donohoe, Timothy J. |
author_sort | Tatton, Matthew R. |
collection | PubMed |
description | [Image: see text] The olefin cross-metathesis reaction allows rapid access to 1,5-dicarbonyl intermediates which, upon treatment with a primary or secondary amine, allow the synthesis of a range of multisubstituted carbocyclic aryl amines. This de novo arene synthesis yields nonclassical substitution patterns in a regioselective and predictable approach that is compatible with several functional groups. |
format | Online Article Text |
id | pubmed-3979090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39790902014-04-08 De Novo Synthesis of Multisubstituted Aryl Amines Using Alkene Cross Metathesis Tatton, Matthew R. Simpson, Iain Donohoe, Timothy J. Org Lett [Image: see text] The olefin cross-metathesis reaction allows rapid access to 1,5-dicarbonyl intermediates which, upon treatment with a primary or secondary amine, allow the synthesis of a range of multisubstituted carbocyclic aryl amines. This de novo arene synthesis yields nonclassical substitution patterns in a regioselective and predictable approach that is compatible with several functional groups. American Chemical Society 2014-03-19 2014-04-04 /pmc/articles/PMC3979090/ /pubmed/24646289 http://dx.doi.org/10.1021/ol500441q Text en Copyright © 2014 American Chemical Society Terms of Use CC-BY (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) |
spellingShingle | Tatton, Matthew R. Simpson, Iain Donohoe, Timothy J. De Novo Synthesis of Multisubstituted Aryl Amines Using Alkene Cross Metathesis |
title | De Novo Synthesis of Multisubstituted Aryl Amines
Using Alkene Cross Metathesis |
title_full | De Novo Synthesis of Multisubstituted Aryl Amines
Using Alkene Cross Metathesis |
title_fullStr | De Novo Synthesis of Multisubstituted Aryl Amines
Using Alkene Cross Metathesis |
title_full_unstemmed | De Novo Synthesis of Multisubstituted Aryl Amines
Using Alkene Cross Metathesis |
title_short | De Novo Synthesis of Multisubstituted Aryl Amines
Using Alkene Cross Metathesis |
title_sort | de novo synthesis of multisubstituted aryl amines
using alkene cross metathesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979090/ https://www.ncbi.nlm.nih.gov/pubmed/24646289 http://dx.doi.org/10.1021/ol500441q |
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