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Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides
The carbocupration reactions of heterosubstituted alkynes allow the regio- and stereoselective formation of vinyl organometallic species. N-Alkynylamides (ynamides) are particularly useful substrates for the highly regioselective carbocupration reaction, as they lead to the stereodefined formation o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628878/ https://www.ncbi.nlm.nih.gov/pubmed/23616793 http://dx.doi.org/10.3762/bjoc.9.57 |
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author | Minko, Yury Pasco, Morgane Chechik, Helena Marek, Ilan |
author_facet | Minko, Yury Pasco, Morgane Chechik, Helena Marek, Ilan |
author_sort | Minko, Yury |
collection | PubMed |
description | The carbocupration reactions of heterosubstituted alkynes allow the regio- and stereoselective formation of vinyl organometallic species. N-Alkynylamides (ynamides) are particularly useful substrates for the highly regioselective carbocupration reaction, as they lead to the stereodefined formation of vinylcopper species geminated to the amide moiety. The latter species are involved in numerous synthetically useful transformations leading to valuable building blocks in organic synthesis. Here we describe in full the results of our studies related to the carbometallation reactions of N-alkynylamides. |
format | Online Article Text |
id | pubmed-3628878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-36288782013-04-24 Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides Minko, Yury Pasco, Morgane Chechik, Helena Marek, Ilan Beilstein J Org Chem Full Research Paper The carbocupration reactions of heterosubstituted alkynes allow the regio- and stereoselective formation of vinyl organometallic species. N-Alkynylamides (ynamides) are particularly useful substrates for the highly regioselective carbocupration reaction, as they lead to the stereodefined formation of vinylcopper species geminated to the amide moiety. The latter species are involved in numerous synthetically useful transformations leading to valuable building blocks in organic synthesis. Here we describe in full the results of our studies related to the carbometallation reactions of N-alkynylamides. Beilstein-Institut 2013-03-13 /pmc/articles/PMC3628878/ /pubmed/23616793 http://dx.doi.org/10.3762/bjoc.9.57 Text en Copyright © 2013, Minko et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Minko, Yury Pasco, Morgane Chechik, Helena Marek, Ilan Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides |
title | Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides |
title_full | Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides |
title_fullStr | Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides |
title_full_unstemmed | Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides |
title_short | Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides |
title_sort | regio- and stereoselective carbometallation reactions of n-alkynylamides and sulfonamides |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628878/ https://www.ncbi.nlm.nih.gov/pubmed/23616793 http://dx.doi.org/10.3762/bjoc.9.57 |
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