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Direct 1,1-Bisphosphonation of Isocyanides: Atom- and Step-Economical Access to Bisphosphinoylaminomethanes
[Image: see text] An atom- and step-economical strategy for the synthesis of bisphosphinoylaminomethanes is reported. This metal-free bisphosphinylation reaction proceeded smoothly through a base-mediated direct 1,1-bisphosphonation of phosphine oxides and isocyanides under mild conditions. The pres...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015124/ https://www.ncbi.nlm.nih.gov/pubmed/33817511 http://dx.doi.org/10.1021/acsomega.1c00160 |
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author | Yuan, Qing Liu, Hua-Wei Cai, Zhong-Jian Ji, Shun-Jun |
author_facet | Yuan, Qing Liu, Hua-Wei Cai, Zhong-Jian Ji, Shun-Jun |
author_sort | Yuan, Qing |
collection | PubMed |
description | [Image: see text] An atom- and step-economical strategy for the synthesis of bisphosphinoylaminomethanes is reported. This metal-free bisphosphinylation reaction proceeded smoothly through a base-mediated direct 1,1-bisphosphonation of phosphine oxides and isocyanides under mild conditions. The present method offers a facile, efficient, and general approach to a broad range of bisphosphinoylaminomethane derivatives in moderate to good yields. |
format | Online Article Text |
id | pubmed-8015124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80151242021-04-02 Direct 1,1-Bisphosphonation of Isocyanides: Atom- and Step-Economical Access to Bisphosphinoylaminomethanes Yuan, Qing Liu, Hua-Wei Cai, Zhong-Jian Ji, Shun-Jun ACS Omega [Image: see text] An atom- and step-economical strategy for the synthesis of bisphosphinoylaminomethanes is reported. This metal-free bisphosphinylation reaction proceeded smoothly through a base-mediated direct 1,1-bisphosphonation of phosphine oxides and isocyanides under mild conditions. The present method offers a facile, efficient, and general approach to a broad range of bisphosphinoylaminomethane derivatives in moderate to good yields. American Chemical Society 2021-03-17 /pmc/articles/PMC8015124/ /pubmed/33817511 http://dx.doi.org/10.1021/acsomega.1c00160 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Yuan, Qing Liu, Hua-Wei Cai, Zhong-Jian Ji, Shun-Jun Direct 1,1-Bisphosphonation of Isocyanides: Atom- and Step-Economical Access to Bisphosphinoylaminomethanes |
title | Direct 1,1-Bisphosphonation of Isocyanides: Atom-
and Step-Economical Access to Bisphosphinoylaminomethanes |
title_full | Direct 1,1-Bisphosphonation of Isocyanides: Atom-
and Step-Economical Access to Bisphosphinoylaminomethanes |
title_fullStr | Direct 1,1-Bisphosphonation of Isocyanides: Atom-
and Step-Economical Access to Bisphosphinoylaminomethanes |
title_full_unstemmed | Direct 1,1-Bisphosphonation of Isocyanides: Atom-
and Step-Economical Access to Bisphosphinoylaminomethanes |
title_short | Direct 1,1-Bisphosphonation of Isocyanides: Atom-
and Step-Economical Access to Bisphosphinoylaminomethanes |
title_sort | direct 1,1-bisphosphonation of isocyanides: atom-
and step-economical access to bisphosphinoylaminomethanes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015124/ https://www.ncbi.nlm.nih.gov/pubmed/33817511 http://dx.doi.org/10.1021/acsomega.1c00160 |
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