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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...

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Autores principales: Minko, Yury, Pasco, Morgane, Chechik, Helena, Marek, Ilan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
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.
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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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