An Efficient One‐Pot Synthesis of 7,7‐Dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one Derivatives Using Chitosan–SO 3 H as Biodegradable Organocatalyst

Chitosan sulfonic acid (CS–SO 3 H), a biodegradable green catalyst, was found to be an impressive system for one‐pot four‐component reaction of different aromatic aldehydes, 3‐acetylcoumarin, dimedone, and ammonium acetate leading to 7,7‐dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinoli...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of heterocyclic chemistry 2019-03, Vol.56 (3), p.947-955
Hauptverfasser: Perumal, Rajasekar, Bathrinarayanan, Balaji, Ghashang, Majid, Mansoor, Syed Sheik
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 955
container_issue 3
container_start_page 947
container_title Journal of heterocyclic chemistry
container_volume 56
creator Perumal, Rajasekar
Bathrinarayanan, Balaji
Ghashang, Majid
Mansoor, Syed Sheik
description Chitosan sulfonic acid (CS–SO 3 H), a biodegradable green catalyst, was found to be an impressive system for one‐pot four‐component reaction of different aromatic aldehydes, 3‐acetylcoumarin, dimedone, and ammonium acetate leading to 7,7‐dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one under solvent‐free condition. This methodology produces diverse superiorities such as operational simplicity, short reaction time, and high yield. Further, the catalyst can be reused for four times without any noticeable decrease in the catalytic activity.
doi_str_mv 10.1002/jhet.3473
format Article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1002_jhet_3473</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1002_jhet_3473</sourcerecordid><originalsourceid>FETCH-LOGICAL-c144t-8fb30f2464d7d3bb48e8dfcc4edb512edd314c4ac50e17af9de6fc337eba67873</originalsourceid><addsrcrecordid>eNotUctKxDAUDaLgOLrwD7JUsNo06aSz1BlfIIwwCu5KmtxMI51Ekyh25ycIfpp_4JeYqotz7uvcC5eD0D7Jj0meFyePLcRjyjjdQCMyZTQryZRuolGaFRkpi4dttBPCYyoJ5XyEvk4tPtfaSAM24oWF7_ePWxfxsrexhWACdhrzI57ac7OG2PZdSouEg4HcmxtKfIVTkK13a7Apowl9d5iYJQj_u8SPqsTKtL3y7vnFWNeZQVweTNL-IHYW8By8eRXRvELA98HYFZ61JrogkvRzucA0aUXAZ8YpWHmhRNMBXviVsE6KKLo-xF20pUUXYO8_jtH9xfnd7Cq7WVxez05vMkkYi1mlG5rrgk2Y4oo2DaugUlpKBqopSQFKUcIkE7LMgXChpwomWlLKoRETXnE6Rod_d6V3IXjQ9ZM36_RtTfJ6cKMe3KgHN-gPVgyPKQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>An Efficient One‐Pot Synthesis of 7,7‐Dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one Derivatives Using Chitosan–SO 3 H as Biodegradable Organocatalyst</title><source>Access via Wiley Online Library</source><creator>Perumal, Rajasekar ; Bathrinarayanan, Balaji ; Ghashang, Majid ; Mansoor, Syed Sheik</creator><creatorcontrib>Perumal, Rajasekar ; Bathrinarayanan, Balaji ; Ghashang, Majid ; Mansoor, Syed Sheik</creatorcontrib><description>Chitosan sulfonic acid (CS–SO 3 H), a biodegradable green catalyst, was found to be an impressive system for one‐pot four‐component reaction of different aromatic aldehydes, 3‐acetylcoumarin, dimedone, and ammonium acetate leading to 7,7‐dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one under solvent‐free condition. This methodology produces diverse superiorities such as operational simplicity, short reaction time, and high yield. Further, the catalyst can be reused for four times without any noticeable decrease in the catalytic activity.</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.3473</identifier><language>eng</language><ispartof>Journal of heterocyclic chemistry, 2019-03, Vol.56 (3), p.947-955</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c144t-8fb30f2464d7d3bb48e8dfcc4edb512edd314c4ac50e17af9de6fc337eba67873</citedby><cites>FETCH-LOGICAL-c144t-8fb30f2464d7d3bb48e8dfcc4edb512edd314c4ac50e17af9de6fc337eba67873</cites><orcidid>0000-0002-7959-6438 ; 0000-0002-4654-0454</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids></links><search><creatorcontrib>Perumal, Rajasekar</creatorcontrib><creatorcontrib>Bathrinarayanan, Balaji</creatorcontrib><creatorcontrib>Ghashang, Majid</creatorcontrib><creatorcontrib>Mansoor, Syed Sheik</creatorcontrib><title>An Efficient One‐Pot Synthesis of 7,7‐Dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one Derivatives Using Chitosan–SO 3 H as Biodegradable Organocatalyst</title><title>Journal of heterocyclic chemistry</title><description>Chitosan sulfonic acid (CS–SO 3 H), a biodegradable green catalyst, was found to be an impressive system for one‐pot four‐component reaction of different aromatic aldehydes, 3‐acetylcoumarin, dimedone, and ammonium acetate leading to 7,7‐dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one under solvent‐free condition. This methodology produces diverse superiorities such as operational simplicity, short reaction time, and high yield. Further, the catalyst can be reused for four times without any noticeable decrease in the catalytic activity.</description><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNotUctKxDAUDaLgOLrwD7JUsNo06aSz1BlfIIwwCu5KmtxMI51Ekyh25ycIfpp_4JeYqotz7uvcC5eD0D7Jj0meFyePLcRjyjjdQCMyZTQryZRuolGaFRkpi4dttBPCYyoJ5XyEvk4tPtfaSAM24oWF7_ePWxfxsrexhWACdhrzI57ac7OG2PZdSouEg4HcmxtKfIVTkK13a7Apowl9d5iYJQj_u8SPqsTKtL3y7vnFWNeZQVweTNL-IHYW8By8eRXRvELA98HYFZ61JrogkvRzucA0aUXAZ8YpWHmhRNMBXviVsE6KKLo-xF20pUUXYO8_jtH9xfnd7Cq7WVxez05vMkkYi1mlG5rrgk2Y4oo2DaugUlpKBqopSQFKUcIkE7LMgXChpwomWlLKoRETXnE6Rod_d6V3IXjQ9ZM36_RtTfJ6cKMe3KgHN-gPVgyPKQ</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Perumal, Rajasekar</creator><creator>Bathrinarayanan, Balaji</creator><creator>Ghashang, Majid</creator><creator>Mansoor, Syed Sheik</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-7959-6438</orcidid><orcidid>https://orcid.org/0000-0002-4654-0454</orcidid></search><sort><creationdate>201903</creationdate><title>An Efficient One‐Pot Synthesis of 7,7‐Dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one Derivatives Using Chitosan–SO 3 H as Biodegradable Organocatalyst</title><author>Perumal, Rajasekar ; Bathrinarayanan, Balaji ; Ghashang, Majid ; Mansoor, Syed Sheik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c144t-8fb30f2464d7d3bb48e8dfcc4edb512edd314c4ac50e17af9de6fc337eba67873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Perumal, Rajasekar</creatorcontrib><creatorcontrib>Bathrinarayanan, Balaji</creatorcontrib><creatorcontrib>Ghashang, Majid</creatorcontrib><creatorcontrib>Mansoor, Syed Sheik</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Perumal, Rajasekar</au><au>Bathrinarayanan, Balaji</au><au>Ghashang, Majid</au><au>Mansoor, Syed Sheik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An Efficient One‐Pot Synthesis of 7,7‐Dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one Derivatives Using Chitosan–SO 3 H as Biodegradable Organocatalyst</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><date>2019-03</date><risdate>2019</risdate><volume>56</volume><issue>3</issue><spage>947</spage><epage>955</epage><pages>947-955</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>Chitosan sulfonic acid (CS–SO 3 H), a biodegradable green catalyst, was found to be an impressive system for one‐pot four‐component reaction of different aromatic aldehydes, 3‐acetylcoumarin, dimedone, and ammonium acetate leading to 7,7‐dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one under solvent‐free condition. This methodology produces diverse superiorities such as operational simplicity, short reaction time, and high yield. Further, the catalyst can be reused for four times without any noticeable decrease in the catalytic activity.</abstract><doi>10.1002/jhet.3473</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7959-6438</orcidid><orcidid>https://orcid.org/0000-0002-4654-0454</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0022-152X
ispartof Journal of heterocyclic chemistry, 2019-03, Vol.56 (3), p.947-955
issn 0022-152X
1943-5193
language eng
recordid cdi_crossref_primary_10_1002_jhet_3473
source Access via Wiley Online Library
title An Efficient One‐Pot Synthesis of 7,7‐Dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one Derivatives Using Chitosan–SO 3 H as Biodegradable Organocatalyst
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T19%3A34%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=An%20Efficient%20One%E2%80%90Pot%20Synthesis%20of%207,7%E2%80%90Dimethyl%E2%80%902%E2%80%90(2%E2%80%90oxo%E2%80%902%20H%20%E2%80%90chromen%E2%80%903%E2%80%90yl)%E2%80%904%E2%80%90aryl%E2%80%907,8%E2%80%90dihydroquinolin%E2%80%905(6%20H%20)%E2%80%90one%20Derivatives%20Using%20Chitosan%E2%80%93SO%203%20H%20as%20Biodegradable%20Organocatalyst&rft.jtitle=Journal%20of%20heterocyclic%20chemistry&rft.au=Perumal,%20Rajasekar&rft.date=2019-03&rft.volume=56&rft.issue=3&rft.spage=947&rft.epage=955&rft.pages=947-955&rft.issn=0022-152X&rft.eissn=1943-5193&rft_id=info:doi/10.1002/jhet.3473&rft_dat=%3Ccrossref%3E10_1002_jhet_3473%3C/crossref%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