Preparation of pyran derivatives promoted by FeCl3.6H2O in ionic liquid

The condensation reaction of chalcone and 1,3-cyclohexanedione was smoothly carried out in [bmim][BF4] with catalysis by FeCl3.6H2O. A series of substituted pyrans were obtained by this reaction, in high yields under mild conditions through a simple operational procedure. In addition, the ionic liqu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of chemical research 2008-06, Vol.2008 (6), p.357-360
Hauptverfasser: Zhang, Xinying, Lv, Quanjian, Fan, Xuesen, Qu, Guirong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 360
container_issue 6
container_start_page 357
container_title Journal of chemical research
container_volume 2008
creator Zhang, Xinying
Lv, Quanjian
Fan, Xuesen
Qu, Guirong
description The condensation reaction of chalcone and 1,3-cyclohexanedione was smoothly carried out in [bmim][BF4] with catalysis by FeCl3.6H2O. A series of substituted pyrans were obtained by this reaction, in high yields under mild conditions through a simple operational procedure. In addition, the ionic liquid together with the catalyst used can be conveniently recovered and efficiently reused.
doi_str_mv 10.3184/030823408X324715
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_1494356384</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1494356384</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_14943563843</originalsourceid><addsrcrecordid>eNqVi70OgjAURhujifizO97RBW1pC2UmopsODm6myjWpqRRbIPHtZfAFnM6Xk-8QsmJ0w5kSW8qpSrig6sITkTE5IlFCRRankmZjErFs2JLlakpmITwpFTLNWUT2J4-N9ro1rgb3gObjdQ0VetMPrscAjXcv12IFtw-UWFi-SQ_JEUwNQ2LuYM27M9WCTB7aBlz-OCfrcncuDvGQvzsM7fVlwh2t1TW6LlyZyAWXKVeC_3H9Ar57RUw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1494356384</pqid></control><display><type>article</type><title>Preparation of pyran derivatives promoted by FeCl3.6H2O in ionic liquid</title><source>Sage Journals GOLD Open Access 2024</source><source>Alma/SFX Local Collection</source><creator>Zhang, Xinying ; Lv, Quanjian ; Fan, Xuesen ; Qu, Guirong</creator><creatorcontrib>Zhang, Xinying ; Lv, Quanjian ; Fan, Xuesen ; Qu, Guirong</creatorcontrib><description>The condensation reaction of chalcone and 1,3-cyclohexanedione was smoothly carried out in [bmim][BF4] with catalysis by FeCl3.6H2O. A series of substituted pyrans were obtained by this reaction, in high yields under mild conditions through a simple operational procedure. In addition, the ionic liquid together with the catalyst used can be conveniently recovered and efficiently reused.</description><identifier>ISSN: 1747-5198</identifier><identifier>EISSN: 2047-6507</identifier><identifier>DOI: 10.3184/030823408X324715</identifier><language>eng</language><subject>Catalysis</subject><ispartof>Journal of chemical research, 2008-06, Vol.2008 (6), p.357-360</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Zhang, Xinying</creatorcontrib><creatorcontrib>Lv, Quanjian</creatorcontrib><creatorcontrib>Fan, Xuesen</creatorcontrib><creatorcontrib>Qu, Guirong</creatorcontrib><title>Preparation of pyran derivatives promoted by FeCl3.6H2O in ionic liquid</title><title>Journal of chemical research</title><description>The condensation reaction of chalcone and 1,3-cyclohexanedione was smoothly carried out in [bmim][BF4] with catalysis by FeCl3.6H2O. A series of substituted pyrans were obtained by this reaction, in high yields under mild conditions through a simple operational procedure. In addition, the ionic liquid together with the catalyst used can be conveniently recovered and efficiently reused.</description><subject>Catalysis</subject><issn>1747-5198</issn><issn>2047-6507</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqVi70OgjAURhujifizO97RBW1pC2UmopsODm6myjWpqRRbIPHtZfAFnM6Xk-8QsmJ0w5kSW8qpSrig6sITkTE5IlFCRRankmZjErFs2JLlakpmITwpFTLNWUT2J4-N9ro1rgb3gObjdQ0VetMPrscAjXcv12IFtw-UWFi-SQ_JEUwNQ2LuYM27M9WCTB7aBlz-OCfrcncuDvGQvzsM7fVlwh2t1TW6LlyZyAWXKVeC_3H9Ar57RUw</recordid><startdate>20080601</startdate><enddate>20080601</enddate><creator>Zhang, Xinying</creator><creator>Lv, Quanjian</creator><creator>Fan, Xuesen</creator><creator>Qu, Guirong</creator><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20080601</creationdate><title>Preparation of pyran derivatives promoted by FeCl3.6H2O in ionic liquid</title><author>Zhang, Xinying ; Lv, Quanjian ; Fan, Xuesen ; Qu, Guirong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_14943563843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Catalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Xinying</creatorcontrib><creatorcontrib>Lv, Quanjian</creatorcontrib><creatorcontrib>Fan, Xuesen</creatorcontrib><creatorcontrib>Qu, Guirong</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of chemical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Xinying</au><au>Lv, Quanjian</au><au>Fan, Xuesen</au><au>Qu, Guirong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of pyran derivatives promoted by FeCl3.6H2O in ionic liquid</atitle><jtitle>Journal of chemical research</jtitle><date>2008-06-01</date><risdate>2008</risdate><volume>2008</volume><issue>6</issue><spage>357</spage><epage>360</epage><pages>357-360</pages><issn>1747-5198</issn><eissn>2047-6507</eissn><abstract>The condensation reaction of chalcone and 1,3-cyclohexanedione was smoothly carried out in [bmim][BF4] with catalysis by FeCl3.6H2O. A series of substituted pyrans were obtained by this reaction, in high yields under mild conditions through a simple operational procedure. In addition, the ionic liquid together with the catalyst used can be conveniently recovered and efficiently reused.</abstract><doi>10.3184/030823408X324715</doi></addata></record>
fulltext fulltext
identifier ISSN: 1747-5198
ispartof Journal of chemical research, 2008-06, Vol.2008 (6), p.357-360
issn 1747-5198
2047-6507
language eng
recordid cdi_proquest_miscellaneous_1494356384
source Sage Journals GOLD Open Access 2024; Alma/SFX Local Collection
subjects Catalysis
title Preparation of pyran derivatives promoted by FeCl3.6H2O in ionic liquid
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T02%3A38%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Preparation%20of%20pyran%20derivatives%20promoted%20by%20FeCl3.6H2O%20in%20ionic%20liquid&rft.jtitle=Journal%20of%20chemical%20research&rft.au=Zhang,%20Xinying&rft.date=2008-06-01&rft.volume=2008&rft.issue=6&rft.spage=357&rft.epage=360&rft.pages=357-360&rft.issn=1747-5198&rft.eissn=2047-6507&rft_id=info:doi/10.3184/030823408X324715&rft_dat=%3Cproquest%3E1494356384%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1494356384&rft_id=info:pmid/&rfr_iscdi=true