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A review on lawsone-based benzo[a]phenazin-5-ol: synthetic approaches and reactions
Phenazine systems are an important class of aza-polycyclic compounds that are easily found in nature and isolated as secondary metabolites primarily from Pseudomonas, Streptomyces, and a few other genera from soil or marine habitats. Moreover, various synthetic phenazine analogs are known for their...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082651/ https://www.ncbi.nlm.nih.gov/pubmed/35541431 http://dx.doi.org/10.1039/d2ra02139k |
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author | Olyaei, Abolfazl Sadeghpour, Mahdieh |
author_facet | Olyaei, Abolfazl Sadeghpour, Mahdieh |
author_sort | Olyaei, Abolfazl |
collection | PubMed |
description | Phenazine systems are an important class of aza-polycyclic compounds that are easily found in nature and isolated as secondary metabolites primarily from Pseudomonas, Streptomyces, and a few other genera from soil or marine habitats. Moreover, various synthetic phenazine analogs are known for their pharmaceutical activities. Among various phenazines, benzo[a]phenazines are structural subunits in a variety of important natural products and have been given special attention due to their unique biological properties in various fields. In this review article, we highlight the synthesis of benzo[a]phenazin-5-ol derivatives from lawsone and benzene-1,2-diamines and their applications for the construction of a variety of five and six membered fused heterocycles such as pyranophenazines, spiropyranophenazines, pyridophenazines, furophenazines, benzochromenophenazines and oxazinophenazines during the period of 1995 to 2021. |
format | Online Article Text |
id | pubmed-9082651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90826512022-05-09 A review on lawsone-based benzo[a]phenazin-5-ol: synthetic approaches and reactions Olyaei, Abolfazl Sadeghpour, Mahdieh RSC Adv Chemistry Phenazine systems are an important class of aza-polycyclic compounds that are easily found in nature and isolated as secondary metabolites primarily from Pseudomonas, Streptomyces, and a few other genera from soil or marine habitats. Moreover, various synthetic phenazine analogs are known for their pharmaceutical activities. Among various phenazines, benzo[a]phenazines are structural subunits in a variety of important natural products and have been given special attention due to their unique biological properties in various fields. In this review article, we highlight the synthesis of benzo[a]phenazin-5-ol derivatives from lawsone and benzene-1,2-diamines and their applications for the construction of a variety of five and six membered fused heterocycles such as pyranophenazines, spiropyranophenazines, pyridophenazines, furophenazines, benzochromenophenazines and oxazinophenazines during the period of 1995 to 2021. The Royal Society of Chemistry 2022-05-09 /pmc/articles/PMC9082651/ /pubmed/35541431 http://dx.doi.org/10.1039/d2ra02139k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Olyaei, Abolfazl Sadeghpour, Mahdieh A review on lawsone-based benzo[a]phenazin-5-ol: synthetic approaches and reactions |
title | A review on lawsone-based benzo[a]phenazin-5-ol: synthetic approaches and reactions |
title_full | A review on lawsone-based benzo[a]phenazin-5-ol: synthetic approaches and reactions |
title_fullStr | A review on lawsone-based benzo[a]phenazin-5-ol: synthetic approaches and reactions |
title_full_unstemmed | A review on lawsone-based benzo[a]phenazin-5-ol: synthetic approaches and reactions |
title_short | A review on lawsone-based benzo[a]phenazin-5-ol: synthetic approaches and reactions |
title_sort | review on lawsone-based benzo[a]phenazin-5-ol: synthetic approaches and reactions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082651/ https://www.ncbi.nlm.nih.gov/pubmed/35541431 http://dx.doi.org/10.1039/d2ra02139k |
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