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A Ni-catalyzed asymmetric C(sp)–P cross-coupling reaction for the synthesis of P-stereogenic alkynylphosphines

Due to the high reactivity of the triple bond, P-stereogenic alkynylphosphines could be easily derivatized, serving as universal building blocks for structurally diverse phosphine compounds. However, the synthesis of alkynylphosphines via direct P–C bond formation was unprecedented. Here, we report...

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Detalles Bibliográficos
Autores principales: Zhang, Bin, Zhou, Wen-Qing, Liu, Xu-Teng, Sun, Yingying, Zhang, Qing-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891383/
https://www.ncbi.nlm.nih.gov/pubmed/36756330
http://dx.doi.org/10.1039/d2sc05841c
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author Zhang, Bin
Zhou, Wen-Qing
Liu, Xu-Teng
Sun, Yingying
Zhang, Qing-Wei
author_facet Zhang, Bin
Zhou, Wen-Qing
Liu, Xu-Teng
Sun, Yingying
Zhang, Qing-Wei
author_sort Zhang, Bin
collection PubMed
description Due to the high reactivity of the triple bond, P-stereogenic alkynylphosphines could be easily derivatized, serving as universal building blocks for structurally diverse phosphine compounds. However, the synthesis of alkynylphosphines via direct P–C bond formation was unprecedented. Here, we report an efficient method for the synthesis of P-stereogenic alkynylphosphines with high enantioselectivity via a Ni-catalyzed asymmetric cross-coupling reaction. The reaction could tolerate a variety of functional groups, affording products that can be converted into useful phosphine derivatives.
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spelling pubmed-98913832023-02-07 A Ni-catalyzed asymmetric C(sp)–P cross-coupling reaction for the synthesis of P-stereogenic alkynylphosphines Zhang, Bin Zhou, Wen-Qing Liu, Xu-Teng Sun, Yingying Zhang, Qing-Wei Chem Sci Chemistry Due to the high reactivity of the triple bond, P-stereogenic alkynylphosphines could be easily derivatized, serving as universal building blocks for structurally diverse phosphine compounds. However, the synthesis of alkynylphosphines via direct P–C bond formation was unprecedented. Here, we report an efficient method for the synthesis of P-stereogenic alkynylphosphines with high enantioselectivity via a Ni-catalyzed asymmetric cross-coupling reaction. The reaction could tolerate a variety of functional groups, affording products that can be converted into useful phosphine derivatives. The Royal Society of Chemistry 2023-01-07 /pmc/articles/PMC9891383/ /pubmed/36756330 http://dx.doi.org/10.1039/d2sc05841c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhang, Bin
Zhou, Wen-Qing
Liu, Xu-Teng
Sun, Yingying
Zhang, Qing-Wei
A Ni-catalyzed asymmetric C(sp)–P cross-coupling reaction for the synthesis of P-stereogenic alkynylphosphines
title A Ni-catalyzed asymmetric C(sp)–P cross-coupling reaction for the synthesis of P-stereogenic alkynylphosphines
title_full A Ni-catalyzed asymmetric C(sp)–P cross-coupling reaction for the synthesis of P-stereogenic alkynylphosphines
title_fullStr A Ni-catalyzed asymmetric C(sp)–P cross-coupling reaction for the synthesis of P-stereogenic alkynylphosphines
title_full_unstemmed A Ni-catalyzed asymmetric C(sp)–P cross-coupling reaction for the synthesis of P-stereogenic alkynylphosphines
title_short A Ni-catalyzed asymmetric C(sp)–P cross-coupling reaction for the synthesis of P-stereogenic alkynylphosphines
title_sort ni-catalyzed asymmetric c(sp)–p cross-coupling reaction for the synthesis of p-stereogenic alkynylphosphines
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891383/
https://www.ncbi.nlm.nih.gov/pubmed/36756330
http://dx.doi.org/10.1039/d2sc05841c
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