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Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates

A novel class of cyclic phosphine derived bifunctional catalysts (Le-Phos) is reported, which can be readily prepared from inexpensive and commercially available starting materials and exhibit good performances in enantioselective γ-addition reactions of N-centered nucleophiles and allenoates under...

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Detalles Bibliográficos
Autores principales: Qiu, Haile, Chen, Xiaofeng, Zhang, Junliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988743/
https://www.ncbi.nlm.nih.gov/pubmed/32055374
http://dx.doi.org/10.1039/c9sc04073k
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author Qiu, Haile
Chen, Xiaofeng
Zhang, Junliang
author_facet Qiu, Haile
Chen, Xiaofeng
Zhang, Junliang
author_sort Qiu, Haile
collection PubMed
description A novel class of cyclic phosphine derived bifunctional catalysts (Le-Phos) is reported, which can be readily prepared from inexpensive and commercially available starting materials and exhibit good performances in enantioselective γ-addition reactions of N-centered nucleophiles and allenoates under mild conditions. The salient features of this reaction include high product yields, good enantioselectivity, mild reaction conditions, and broad substrate scope and gram-scale scalability.
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spelling pubmed-69887432020-02-13 Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates Qiu, Haile Chen, Xiaofeng Zhang, Junliang Chem Sci Chemistry A novel class of cyclic phosphine derived bifunctional catalysts (Le-Phos) is reported, which can be readily prepared from inexpensive and commercially available starting materials and exhibit good performances in enantioselective γ-addition reactions of N-centered nucleophiles and allenoates under mild conditions. The salient features of this reaction include high product yields, good enantioselectivity, mild reaction conditions, and broad substrate scope and gram-scale scalability. Royal Society of Chemistry 2019-09-03 /pmc/articles/PMC6988743/ /pubmed/32055374 http://dx.doi.org/10.1039/c9sc04073k Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Qiu, Haile
Chen, Xiaofeng
Zhang, Junliang
Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates
title Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates
title_full Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates
title_fullStr Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates
title_full_unstemmed Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates
title_short Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates
title_sort design, synthesis and application of a new type of bifunctional le-phos in highly enantioselective γ-addition reactions of n-centered nucleophiles to allenoates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988743/
https://www.ncbi.nlm.nih.gov/pubmed/32055374
http://dx.doi.org/10.1039/c9sc04073k
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