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N-Heterocyclic carbenes as chiral Brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction

Highly diastereo- and enantioselective 1,6-addition of 1,3-ketoamides to p-quinone methides (p-QMs) using chiral NHCs as Brønsted base catalysts is developed. The reaction is based on the utilization of a 1,3-ketoamide having acidic N–H that forms a chiral ion-pair consisting of the enolate and the...

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Detalles Bibliográficos
Autores principales: Santra, Surojit, Porey, Arka, Jana, Barun, Guin, Joyram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144034/
https://www.ncbi.nlm.nih.gov/pubmed/30288232
http://dx.doi.org/10.1039/c8sc02138d
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author Santra, Surojit
Porey, Arka
Jana, Barun
Guin, Joyram
author_facet Santra, Surojit
Porey, Arka
Jana, Barun
Guin, Joyram
author_sort Santra, Surojit
collection PubMed
description Highly diastereo- and enantioselective 1,6-addition of 1,3-ketoamides to p-quinone methides (p-QMs) using chiral NHCs as Brønsted base catalysts is developed. The reaction is based on the utilization of a 1,3-ketoamide having acidic N–H that forms a chiral ion-pair consisting of the enolate and the azolium ion. Different β-ketoamides and functionalized p-QMs are applicable to the reaction. Synthetic application of the method is demonstrated via the preparation of highly enantioenriched β and γ-lactam derivatives.
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spelling pubmed-61440342018-10-04 N-Heterocyclic carbenes as chiral Brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction Santra, Surojit Porey, Arka Jana, Barun Guin, Joyram Chem Sci Chemistry Highly diastereo- and enantioselective 1,6-addition of 1,3-ketoamides to p-quinone methides (p-QMs) using chiral NHCs as Brønsted base catalysts is developed. The reaction is based on the utilization of a 1,3-ketoamide having acidic N–H that forms a chiral ion-pair consisting of the enolate and the azolium ion. Different β-ketoamides and functionalized p-QMs are applicable to the reaction. Synthetic application of the method is demonstrated via the preparation of highly enantioenriched β and γ-lactam derivatives. Royal Society of Chemistry 2018-07-02 /pmc/articles/PMC6144034/ /pubmed/30288232 http://dx.doi.org/10.1039/c8sc02138d Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Santra, Surojit
Porey, Arka
Jana, Barun
Guin, Joyram
N-Heterocyclic carbenes as chiral Brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction
title N-Heterocyclic carbenes as chiral Brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction
title_full N-Heterocyclic carbenes as chiral Brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction
title_fullStr N-Heterocyclic carbenes as chiral Brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction
title_full_unstemmed N-Heterocyclic carbenes as chiral Brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction
title_short N-Heterocyclic carbenes as chiral Brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction
title_sort n-heterocyclic carbenes as chiral brønsted base catalysts: a highly diastereo- and enantioselective 1,6-addition reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144034/
https://www.ncbi.nlm.nih.gov/pubmed/30288232
http://dx.doi.org/10.1039/c8sc02138d
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