Reusable Nano Catalysed Synthesis of Heterocycles: An Overview

The field of reusable nano‐catalysts has grown rapidly over the last decade. Recently, transition metal catalysed organic reactions have attracted considerable interest from the pharmaceutical and organic chemistry fields. Synthetic procedures based on such heterogeneous nanocatalysts are easier, le...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ChemistrySelect (Weinheim) 2022-02, Vol.7 (8), p.n/a
Hauptverfasser: Sonawane, Harshad R., Deore, Jaydeep V., Chavan, Pravin N.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page n/a
container_issue 8
container_start_page
container_title ChemistrySelect (Weinheim)
container_volume 7
creator Sonawane, Harshad R.
Deore, Jaydeep V.
Chavan, Pravin N.
description The field of reusable nano‐catalysts has grown rapidly over the last decade. Recently, transition metal catalysed organic reactions have attracted considerable interest from the pharmaceutical and organic chemistry fields. Synthetic procedures based on such heterogeneous nanocatalysts are easier, less expensive, non‐toxic, and eco‐friendly, producing only the most desirable products in higher yields and allowing for easy catalyst separation. Heterogeneous nano‐catalysts were highly preferred over homogeneous catalysts for the synthesis of heterocyclic compounds due to their effective separation processes for both products and catalysts. According to recent studies, nanoparticles (NPs) are commonly used as a heterogeneous catalyst in the production of heterocyclic compounds. Heterogeneous catalysts are widely used in a variety of organic reactions due to their high surface‐to‐volume ratio. Most importantly, after the reaction is complete, easy magnetic separation of the catalyst minimises the requirement for catalyst filtration. Additionally, magnetic NPs, particularly supported magnetic nanocatalysts, have garnered considerable interest in both academic and industrial research due to their effectiveness as alternatives to traditional materials, their ease of separation via an external magnet, and their high degree of chemical stability in a variety of organic and inorganic solvents. To reach its depth, this review is focused on the most recent examples, their preparation, synthetic strategies and recycling studies of highly excited catalytic systems used for the synthesis of heterocyclic compounds. Reusable nanocatalyst. The synthesis of heterocycles with reusable nanocatalysts has recently gotten much attention from the pharmaceutical and organic chemistry fields. Heterocyclic compounds (HC) with five and six members played a vital role in medicinal chemistry. Because of its high surface‐to‐volume ratio, heterogeneous nanocatalysts are frequently utilized in a wide range of organic reactions. The nanocatalyst can be easily separated with magnetic forces and reused many times without losing catalytic activity. Utilizing reusable nanocatalysts reduces catalyst filtration requirements.
doi_str_mv 10.1002/slct.202103900
format Article
fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_slct_202103900</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>SLCT202103900</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2890-570a5de3fd6f25166ed87f89c226fb653465ef72a043460edcab360ad6c463bd3</originalsourceid><addsrcrecordid>eNqFkMFKw0AURQdRsNRuXc8PpL7MZF4SF0IJaoVgwdb1MJl5g5GYSCa25O9taVF3ru5d3HMXh7HrGOYxgLgJjR3mAkQMMgc4YxMhUUWokvz8T79ksxDeASDGDIVKJ-zuhb6CqRriz6bteGEG04yBHF-P7fBGoQ6883xJA_WdHW1D4ZYvWr7aUr-taXfFLrxpAs1OOWWvD_ebYhmVq8enYlFGVmQ5RCoFoxxJ79ALFSOSy1Kf5VYI9BUqmaAinwoDyb4COWsqiWAc2gRl5eSUzY-_tu9C6Mnrz77-MP2oY9AHAfogQP8I2AP5EdjVDY3_rPW6LDa_7De-oV9C</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Reusable Nano Catalysed Synthesis of Heterocycles: An Overview</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Sonawane, Harshad R. ; Deore, Jaydeep V. ; Chavan, Pravin N.</creator><creatorcontrib>Sonawane, Harshad R. ; Deore, Jaydeep V. ; Chavan, Pravin N.</creatorcontrib><description>The field of reusable nano‐catalysts has grown rapidly over the last decade. Recently, transition metal catalysed organic reactions have attracted considerable interest from the pharmaceutical and organic chemistry fields. Synthetic procedures based on such heterogeneous nanocatalysts are easier, less expensive, non‐toxic, and eco‐friendly, producing only the most desirable products in higher yields and allowing for easy catalyst separation. Heterogeneous nano‐catalysts were highly preferred over homogeneous catalysts for the synthesis of heterocyclic compounds due to their effective separation processes for both products and catalysts. According to recent studies, nanoparticles (NPs) are commonly used as a heterogeneous catalyst in the production of heterocyclic compounds. Heterogeneous catalysts are widely used in a variety of organic reactions due to their high surface‐to‐volume ratio. Most importantly, after the reaction is complete, easy magnetic separation of the catalyst minimises the requirement for catalyst filtration. Additionally, magnetic NPs, particularly supported magnetic nanocatalysts, have garnered considerable interest in both academic and industrial research due to their effectiveness as alternatives to traditional materials, their ease of separation via an external magnet, and their high degree of chemical stability in a variety of organic and inorganic solvents. To reach its depth, this review is focused on the most recent examples, their preparation, synthetic strategies and recycling studies of highly excited catalytic systems used for the synthesis of heterocyclic compounds. Reusable nanocatalyst. The synthesis of heterocycles with reusable nanocatalysts has recently gotten much attention from the pharmaceutical and organic chemistry fields. Heterocyclic compounds (HC) with five and six members played a vital role in medicinal chemistry. Because of its high surface‐to‐volume ratio, heterogeneous nanocatalysts are frequently utilized in a wide range of organic reactions. The nanocatalyst can be easily separated with magnetic forces and reused many times without losing catalytic activity. Utilizing reusable nanocatalysts reduces catalyst filtration requirements.</description><identifier>ISSN: 2365-6549</identifier><identifier>EISSN: 2365-6549</identifier><identifier>DOI: 10.1002/slct.202103900</identifier><language>eng</language><subject>Eco-firendly ; Heterocycles ; Multicomponent reactions ; Nano catalyst ; Nanoparticles ; Reusable catalyst</subject><ispartof>ChemistrySelect (Weinheim), 2022-02, Vol.7 (8), p.n/a</ispartof><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2890-570a5de3fd6f25166ed87f89c226fb653465ef72a043460edcab360ad6c463bd3</citedby><cites>FETCH-LOGICAL-c2890-570a5de3fd6f25166ed87f89c226fb653465ef72a043460edcab360ad6c463bd3</cites><orcidid>0000-0002-1232-9343 ; 0000-0002-4763-8226</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fslct.202103900$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fslct.202103900$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Sonawane, Harshad R.</creatorcontrib><creatorcontrib>Deore, Jaydeep V.</creatorcontrib><creatorcontrib>Chavan, Pravin N.</creatorcontrib><title>Reusable Nano Catalysed Synthesis of Heterocycles: An Overview</title><title>ChemistrySelect (Weinheim)</title><description>The field of reusable nano‐catalysts has grown rapidly over the last decade. Recently, transition metal catalysed organic reactions have attracted considerable interest from the pharmaceutical and organic chemistry fields. Synthetic procedures based on such heterogeneous nanocatalysts are easier, less expensive, non‐toxic, and eco‐friendly, producing only the most desirable products in higher yields and allowing for easy catalyst separation. Heterogeneous nano‐catalysts were highly preferred over homogeneous catalysts for the synthesis of heterocyclic compounds due to their effective separation processes for both products and catalysts. According to recent studies, nanoparticles (NPs) are commonly used as a heterogeneous catalyst in the production of heterocyclic compounds. Heterogeneous catalysts are widely used in a variety of organic reactions due to their high surface‐to‐volume ratio. Most importantly, after the reaction is complete, easy magnetic separation of the catalyst minimises the requirement for catalyst filtration. Additionally, magnetic NPs, particularly supported magnetic nanocatalysts, have garnered considerable interest in both academic and industrial research due to their effectiveness as alternatives to traditional materials, their ease of separation via an external magnet, and their high degree of chemical stability in a variety of organic and inorganic solvents. To reach its depth, this review is focused on the most recent examples, their preparation, synthetic strategies and recycling studies of highly excited catalytic systems used for the synthesis of heterocyclic compounds. Reusable nanocatalyst. The synthesis of heterocycles with reusable nanocatalysts has recently gotten much attention from the pharmaceutical and organic chemistry fields. Heterocyclic compounds (HC) with five and six members played a vital role in medicinal chemistry. Because of its high surface‐to‐volume ratio, heterogeneous nanocatalysts are frequently utilized in a wide range of organic reactions. The nanocatalyst can be easily separated with magnetic forces and reused many times without losing catalytic activity. Utilizing reusable nanocatalysts reduces catalyst filtration requirements.</description><subject>Eco-firendly</subject><subject>Heterocycles</subject><subject>Multicomponent reactions</subject><subject>Nano catalyst</subject><subject>Nanoparticles</subject><subject>Reusable catalyst</subject><issn>2365-6549</issn><issn>2365-6549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkMFKw0AURQdRsNRuXc8PpL7MZF4SF0IJaoVgwdb1MJl5g5GYSCa25O9taVF3ru5d3HMXh7HrGOYxgLgJjR3mAkQMMgc4YxMhUUWokvz8T79ksxDeASDGDIVKJ-zuhb6CqRriz6bteGEG04yBHF-P7fBGoQ6883xJA_WdHW1D4ZYvWr7aUr-taXfFLrxpAs1OOWWvD_ebYhmVq8enYlFGVmQ5RCoFoxxJ79ALFSOSy1Kf5VYI9BUqmaAinwoDyb4COWsqiWAc2gRl5eSUzY-_tu9C6Mnrz77-MP2oY9AHAfogQP8I2AP5EdjVDY3_rPW6LDa_7De-oV9C</recordid><startdate>20220224</startdate><enddate>20220224</enddate><creator>Sonawane, Harshad R.</creator><creator>Deore, Jaydeep V.</creator><creator>Chavan, Pravin N.</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-1232-9343</orcidid><orcidid>https://orcid.org/0000-0002-4763-8226</orcidid></search><sort><creationdate>20220224</creationdate><title>Reusable Nano Catalysed Synthesis of Heterocycles: An Overview</title><author>Sonawane, Harshad R. ; Deore, Jaydeep V. ; Chavan, Pravin N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2890-570a5de3fd6f25166ed87f89c226fb653465ef72a043460edcab360ad6c463bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Eco-firendly</topic><topic>Heterocycles</topic><topic>Multicomponent reactions</topic><topic>Nano catalyst</topic><topic>Nanoparticles</topic><topic>Reusable catalyst</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sonawane, Harshad R.</creatorcontrib><creatorcontrib>Deore, Jaydeep V.</creatorcontrib><creatorcontrib>Chavan, Pravin N.</creatorcontrib><collection>CrossRef</collection><jtitle>ChemistrySelect (Weinheim)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sonawane, Harshad R.</au><au>Deore, Jaydeep V.</au><au>Chavan, Pravin N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reusable Nano Catalysed Synthesis of Heterocycles: An Overview</atitle><jtitle>ChemistrySelect (Weinheim)</jtitle><date>2022-02-24</date><risdate>2022</risdate><volume>7</volume><issue>8</issue><epage>n/a</epage><issn>2365-6549</issn><eissn>2365-6549</eissn><abstract>The field of reusable nano‐catalysts has grown rapidly over the last decade. Recently, transition metal catalysed organic reactions have attracted considerable interest from the pharmaceutical and organic chemistry fields. Synthetic procedures based on such heterogeneous nanocatalysts are easier, less expensive, non‐toxic, and eco‐friendly, producing only the most desirable products in higher yields and allowing for easy catalyst separation. Heterogeneous nano‐catalysts were highly preferred over homogeneous catalysts for the synthesis of heterocyclic compounds due to their effective separation processes for both products and catalysts. According to recent studies, nanoparticles (NPs) are commonly used as a heterogeneous catalyst in the production of heterocyclic compounds. Heterogeneous catalysts are widely used in a variety of organic reactions due to their high surface‐to‐volume ratio. Most importantly, after the reaction is complete, easy magnetic separation of the catalyst minimises the requirement for catalyst filtration. Additionally, magnetic NPs, particularly supported magnetic nanocatalysts, have garnered considerable interest in both academic and industrial research due to their effectiveness as alternatives to traditional materials, their ease of separation via an external magnet, and their high degree of chemical stability in a variety of organic and inorganic solvents. To reach its depth, this review is focused on the most recent examples, their preparation, synthetic strategies and recycling studies of highly excited catalytic systems used for the synthesis of heterocyclic compounds. Reusable nanocatalyst. The synthesis of heterocycles with reusable nanocatalysts has recently gotten much attention from the pharmaceutical and organic chemistry fields. Heterocyclic compounds (HC) with five and six members played a vital role in medicinal chemistry. Because of its high surface‐to‐volume ratio, heterogeneous nanocatalysts are frequently utilized in a wide range of organic reactions. The nanocatalyst can be easily separated with magnetic forces and reused many times without losing catalytic activity. Utilizing reusable nanocatalysts reduces catalyst filtration requirements.</abstract><doi>10.1002/slct.202103900</doi><tpages>25</tpages><orcidid>https://orcid.org/0000-0002-1232-9343</orcidid><orcidid>https://orcid.org/0000-0002-4763-8226</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 2365-6549
ispartof ChemistrySelect (Weinheim), 2022-02, Vol.7 (8), p.n/a
issn 2365-6549
2365-6549
language eng
recordid cdi_crossref_primary_10_1002_slct_202103900
source Wiley Online Library Journals Frontfile Complete
subjects Eco-firendly
Heterocycles
Multicomponent reactions
Nano catalyst
Nanoparticles
Reusable catalyst
title Reusable Nano Catalysed Synthesis of Heterocycles: An Overview
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T13%3A09%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Reusable%20Nano%20Catalysed%20Synthesis%20of%20Heterocycles:%20An%20Overview&rft.jtitle=ChemistrySelect%20(Weinheim)&rft.au=Sonawane,%20Harshad%20R.&rft.date=2022-02-24&rft.volume=7&rft.issue=8&rft.epage=n/a&rft.issn=2365-6549&rft.eissn=2365-6549&rft_id=info:doi/10.1002/slct.202103900&rft_dat=%3Cwiley_cross%3ESLCT202103900%3C/wiley_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true