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Production of a recyclable nanobiocatalyst to synthesize quinazolinone derivatives
Nanobiocatalysts (NBCs) are an emerging innovation that paves the way toward sustainable and eco-friendly endeavors. In the quest for a robust and reusable nanobiocatalyst, herein, we report a nanobiocatalyst, namely CALB@MrGO, developed via immobilizing Candida antarctica lipase B onto the surface...
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/PMC9667765/ https://www.ncbi.nlm.nih.gov/pubmed/36425315 http://dx.doi.org/10.1039/d2ra04405f |
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author | Budhiraja, Meenakshi Chudasama, Bhupendra Ali, Amjad Tyagi, Vikas |
author_facet | Budhiraja, Meenakshi Chudasama, Bhupendra Ali, Amjad Tyagi, Vikas |
author_sort | Budhiraja, Meenakshi |
collection | PubMed |
description | Nanobiocatalysts (NBCs) are an emerging innovation that paves the way toward sustainable and eco-friendly endeavors. In the quest for a robust and reusable nanobiocatalyst, herein, we report a nanobiocatalyst, namely CALB@MrGO, developed via immobilizing Candida antarctica lipase B onto the surface of Fe(3)O(4)-decorated reduced graphene oxide (MrGO). Next, the enormous potential of the NBC (CALB@MrGO) was checked by employing it to synthesize clinically important quinazolinone derivatives in good to excellent yield (70–95%) using differently substituted aryl aldehydes with 2-aminobenzamide. Further, the synthetic utility and generality of this protocol was proved by setting up a gram-scale reaction, which afforded the product in 87% yield. The green chemistry metrics calculated for the gram-scale reaction those prove the greenness of this protocol. |
format | Online Article Text |
id | pubmed-9667765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-96677652022-11-23 Production of a recyclable nanobiocatalyst to synthesize quinazolinone derivatives Budhiraja, Meenakshi Chudasama, Bhupendra Ali, Amjad Tyagi, Vikas RSC Adv Chemistry Nanobiocatalysts (NBCs) are an emerging innovation that paves the way toward sustainable and eco-friendly endeavors. In the quest for a robust and reusable nanobiocatalyst, herein, we report a nanobiocatalyst, namely CALB@MrGO, developed via immobilizing Candida antarctica lipase B onto the surface of Fe(3)O(4)-decorated reduced graphene oxide (MrGO). Next, the enormous potential of the NBC (CALB@MrGO) was checked by employing it to synthesize clinically important quinazolinone derivatives in good to excellent yield (70–95%) using differently substituted aryl aldehydes with 2-aminobenzamide. Further, the synthetic utility and generality of this protocol was proved by setting up a gram-scale reaction, which afforded the product in 87% yield. The green chemistry metrics calculated for the gram-scale reaction those prove the greenness of this protocol. The Royal Society of Chemistry 2022-11-16 /pmc/articles/PMC9667765/ /pubmed/36425315 http://dx.doi.org/10.1039/d2ra04405f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Budhiraja, Meenakshi Chudasama, Bhupendra Ali, Amjad Tyagi, Vikas Production of a recyclable nanobiocatalyst to synthesize quinazolinone derivatives |
title | Production of a recyclable nanobiocatalyst to synthesize quinazolinone derivatives |
title_full | Production of a recyclable nanobiocatalyst to synthesize quinazolinone derivatives |
title_fullStr | Production of a recyclable nanobiocatalyst to synthesize quinazolinone derivatives |
title_full_unstemmed | Production of a recyclable nanobiocatalyst to synthesize quinazolinone derivatives |
title_short | Production of a recyclable nanobiocatalyst to synthesize quinazolinone derivatives |
title_sort | production of a recyclable nanobiocatalyst to synthesize quinazolinone derivatives |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667765/ https://www.ncbi.nlm.nih.gov/pubmed/36425315 http://dx.doi.org/10.1039/d2ra04405f |
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