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Recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review
Spiro-heterocycles have received special attention in medicinal chemistry because of their promising biological activity. Over the years, many synthetic methodologies have been established for the construction of spirocyclic compounds. Spiro heterocycles such as spiro-azetidin-2-one, -pyrrolidine, -...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628897/ https://www.ncbi.nlm.nih.gov/pubmed/37942448 http://dx.doi.org/10.1039/d3ra06054c |
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author | Alshammari, Mohammed B. Aly, Ashraf A. Ahmad, Akil Brown, Alan B. Mohamed, Asmaa H. |
author_facet | Alshammari, Mohammed B. Aly, Ashraf A. Ahmad, Akil Brown, Alan B. Mohamed, Asmaa H. |
author_sort | Alshammari, Mohammed B. |
collection | PubMed |
description | Spiro-heterocycles have received special attention in medicinal chemistry because of their promising biological activity. Over the years, many synthetic methodologies have been established for the construction of spirocyclic compounds. Spiro heterocycles such as spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives have been found to exhibit diversified biological and pharmacological activity in addition to their therapeutic properties. In view of these facts, we decided in this review to present representative synthetic approaches of the aforementioned spiro heterocycles, especially in the past 20 years. |
format | Online Article Text |
id | pubmed-10628897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-106288972023-11-08 Recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review Alshammari, Mohammed B. Aly, Ashraf A. Ahmad, Akil Brown, Alan B. Mohamed, Asmaa H. RSC Adv Chemistry Spiro-heterocycles have received special attention in medicinal chemistry because of their promising biological activity. Over the years, many synthetic methodologies have been established for the construction of spirocyclic compounds. Spiro heterocycles such as spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives have been found to exhibit diversified biological and pharmacological activity in addition to their therapeutic properties. In view of these facts, we decided in this review to present representative synthetic approaches of the aforementioned spiro heterocycles, especially in the past 20 years. The Royal Society of Chemistry 2023-11-07 /pmc/articles/PMC10628897/ /pubmed/37942448 http://dx.doi.org/10.1039/d3ra06054c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Alshammari, Mohammed B. Aly, Ashraf A. Ahmad, Akil Brown, Alan B. Mohamed, Asmaa H. Recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review |
title | Recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review |
title_full | Recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review |
title_fullStr | Recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review |
title_full_unstemmed | Recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review |
title_short | Recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review |
title_sort | recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628897/ https://www.ncbi.nlm.nih.gov/pubmed/37942448 http://dx.doi.org/10.1039/d3ra06054c |
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