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Synthesis of medium and large phostams, phostones, and phostines
Phostams, phostones, and phostines are a series of 1,2-azaphosphaheterocycle and 1,2-oxaphosphaheterocycle 2-oxide derivatives. They are phosphorus analogues of lactams and lactones and important biologically active compounds. The strategies for the synthesis of medium and large phostams, phostones,...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204206/ https://www.ncbi.nlm.nih.gov/pubmed/37229219 http://dx.doi.org/10.3762/bjoc.19.50 |
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author | Xu, Jiaxi |
author_facet | Xu, Jiaxi |
author_sort | Xu, Jiaxi |
collection | PubMed |
description | Phostams, phostones, and phostines are a series of 1,2-azaphosphaheterocycle and 1,2-oxaphosphaheterocycle 2-oxide derivatives. They are phosphorus analogues of lactams and lactones and important biologically active compounds. The strategies for the synthesis of medium and large phostams, phostones, and phostines are summarized. They include cyclizations and annulations. Cyclizations achieve ring construction through the formations of C–C, C–O, P–C, and P–O bonds in the rings, while annulations build the rings via [5 + 2], [6 + 1], and [7 + 1] fashions with the stepwise formation of two ring bonds. This review includes the recent syntheses of seven to fourteen-membered phostam, phostone, and phostine derivatives. |
format | Online Article Text |
id | pubmed-10204206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-102042062023-05-24 Synthesis of medium and large phostams, phostones, and phostines Xu, Jiaxi Beilstein J Org Chem Review Phostams, phostones, and phostines are a series of 1,2-azaphosphaheterocycle and 1,2-oxaphosphaheterocycle 2-oxide derivatives. They are phosphorus analogues of lactams and lactones and important biologically active compounds. The strategies for the synthesis of medium and large phostams, phostones, and phostines are summarized. They include cyclizations and annulations. Cyclizations achieve ring construction through the formations of C–C, C–O, P–C, and P–O bonds in the rings, while annulations build the rings via [5 + 2], [6 + 1], and [7 + 1] fashions with the stepwise formation of two ring bonds. This review includes the recent syntheses of seven to fourteen-membered phostam, phostone, and phostine derivatives. Beilstein-Institut 2023-05-15 /pmc/articles/PMC10204206/ /pubmed/37229219 http://dx.doi.org/10.3762/bjoc.19.50 Text en Copyright © 2023, Xu https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material. |
spellingShingle | Review Xu, Jiaxi Synthesis of medium and large phostams, phostones, and phostines |
title | Synthesis of medium and large phostams, phostones, and phostines |
title_full | Synthesis of medium and large phostams, phostones, and phostines |
title_fullStr | Synthesis of medium and large phostams, phostones, and phostines |
title_full_unstemmed | Synthesis of medium and large phostams, phostones, and phostines |
title_short | Synthesis of medium and large phostams, phostones, and phostines |
title_sort | synthesis of medium and large phostams, phostones, and phostines |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204206/ https://www.ncbi.nlm.nih.gov/pubmed/37229219 http://dx.doi.org/10.3762/bjoc.19.50 |
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