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Broad Scope Aminocyclization of Enynes with Cationic JohnPhos–Gold(I) Complex as the Catalyst
[Image: see text] A practical aminocyclization of 1,6-enynes with a wide variety of substituted anilines, including N-alkyl anilines, has been achived by using cationic [JohnPhosAu(MeCN)]SbF(6) as a general purpose catalyst. The resulting adducts can be easily converted into polycyclic compounds by...
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/PMC4782180/ https://www.ncbi.nlm.nih.gov/pubmed/26839084 http://dx.doi.org/10.1021/acs.joc.5b02607 |
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author | Miller, Ricarda Carreras, Javier Muratore, Michael E. Gaydou, Morgane Camponovo, Francesco Echavarren, Antonio M. |
author_facet | Miller, Ricarda Carreras, Javier Muratore, Michael E. Gaydou, Morgane Camponovo, Francesco Echavarren, Antonio M. |
author_sort | Miller, Ricarda |
collection | PubMed |
description | [Image: see text] A practical aminocyclization of 1,6-enynes with a wide variety of substituted anilines, including N-alkyl anilines, has been achived by using cationic [JohnPhosAu(MeCN)]SbF(6) as a general purpose catalyst. The resulting adducts can be easily converted into polycyclic compounds by palladium- and gold-catalyzed reactions. |
format | Online Article Text |
id | pubmed-4782180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-47821802016-03-09 Broad Scope Aminocyclization of Enynes with Cationic JohnPhos–Gold(I) Complex as the Catalyst Miller, Ricarda Carreras, Javier Muratore, Michael E. Gaydou, Morgane Camponovo, Francesco Echavarren, Antonio M. J Org Chem [Image: see text] A practical aminocyclization of 1,6-enynes with a wide variety of substituted anilines, including N-alkyl anilines, has been achived by using cationic [JohnPhosAu(MeCN)]SbF(6) as a general purpose catalyst. The resulting adducts can be easily converted into polycyclic compounds by palladium- and gold-catalyzed reactions. American Chemical Society 2016-02-03 2016-03-04 /pmc/articles/PMC4782180/ /pubmed/26839084 http://dx.doi.org/10.1021/acs.joc.5b02607 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 | Miller, Ricarda Carreras, Javier Muratore, Michael E. Gaydou, Morgane Camponovo, Francesco Echavarren, Antonio M. Broad Scope Aminocyclization of Enynes with Cationic JohnPhos–Gold(I) Complex as the Catalyst |
title | Broad Scope Aminocyclization
of Enynes with Cationic
JohnPhos–Gold(I) Complex as the Catalyst |
title_full | Broad Scope Aminocyclization
of Enynes with Cationic
JohnPhos–Gold(I) Complex as the Catalyst |
title_fullStr | Broad Scope Aminocyclization
of Enynes with Cationic
JohnPhos–Gold(I) Complex as the Catalyst |
title_full_unstemmed | Broad Scope Aminocyclization
of Enynes with Cationic
JohnPhos–Gold(I) Complex as the Catalyst |
title_short | Broad Scope Aminocyclization
of Enynes with Cationic
JohnPhos–Gold(I) Complex as the Catalyst |
title_sort | broad scope aminocyclization
of enynes with cationic
johnphos–gold(i) complex as the catalyst |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782180/ https://www.ncbi.nlm.nih.gov/pubmed/26839084 http://dx.doi.org/10.1021/acs.joc.5b02607 |
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