Green Synthesis of 3-Hydroxynaphthalene-1,4-dione Derivatives via Microwave-Assisted Three-Component Reactions in Neat Water

Green Synthesis of 3-Hydroxynaphthalene-1,4-dione Derivatives via Microwave-Assisted Three-Component Reactions in Neat Water

A novel and efficient access to 2‐(argio(3‐methyl‐5‐oxo‐1‐phenyl‐4,5‐dihydro‐1H‐pyrazol‐4‐yl)methyl)‐3‐hydroxynaphthalene‐1,4‐dione derivatives from readily available substrates in neat water is described with aid of microwave irradiation. The results of our study provide a green, simple and practic...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of heterocyclic chemistry 2012-05, Vol.49 (3), p.521-525
Hauptverfasser: Wang, Shu-Liang, Ding, Jie, Shi, Fen, Liu, Yin-Ping, Jiang, Bo, Ma, Ning, Tu, Shu-Jiang
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 525
container_issue 3
container_start_page 521
container_title Journal of heterocyclic chemistry
container_volume 49
creator Wang, Shu-Liang
Ding, Jie
Shi, Fen
Liu, Yin-Ping
Jiang, Bo
Ma, Ning
Tu, Shu-Jiang
description A novel and efficient access to 2‐(argio(3‐methyl‐5‐oxo‐1‐phenyl‐4,5‐dihydro‐1H‐pyrazol‐4‐yl)methyl)‐3‐hydroxynaphthalene‐1,4‐dione derivatives from readily available substrates in neat water is described with aid of microwave irradiation. The results of our study provide a green, simple and practical one‐pot approach to the synthesis of 3‐hydroxynaphthalene‐1,4‐dione analogs in excellent yields without further purification.
doi_str_mv 10.1002/jhet.798
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1627099424</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3505548491</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3318-b88a862243c1859e81e701139340b5cd040db416f219e720fc41d56c8f5fee473</originalsourceid><addsrcrecordid>eNp1kFFLIzEQx8OhYK0HfoSALz4YzWyym91Hqdoq6h13PTx8CenuLJtad2sSqwt-eFMqgg8-DcP85jfMn5B94MfAeXIybzAcqyL_QQZQSMFSKMQWGcRRwiBN_u-QXe_nsQWh1IC8jR1iS__2bWjQW0-7mgo26SvXvfatWTahMQtskcGRZJXtWqRn6OzKBLtCT1fW0Btbuu7FrJCd-mgIWNFpE61s1D0u40Ib6B80ZYjLntqW3qIJ9M4EdHtkuzYLjz8_6pD8uzifjibs-tf4cnR6zUohIGezPDd5liRSlJCnBeaAigOIQkg-S8uKS17NJGR1AgWqhNelhCrNyrxOa0SpxJAcbLxL1z09ow963j27Np7UkCWKF4WM8iE53FDxHe8d1nrp7KNxvQau19nqdbY6ZhtRtkFf7AL7bzl9NTmffuHX8bx-8sY96EwJleq727H-rW4u7uH-Sp-Jd_3QirM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1627099424</pqid></control><display><type>article</type><title>Green Synthesis of 3-Hydroxynaphthalene-1,4-dione Derivatives via Microwave-Assisted Three-Component Reactions in Neat Water</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Wang, Shu-Liang ; Ding, Jie ; Shi, Fen ; Liu, Yin-Ping ; Jiang, Bo ; Ma, Ning ; Tu, Shu-Jiang</creator><creatorcontrib>Wang, Shu-Liang ; Ding, Jie ; Shi, Fen ; Liu, Yin-Ping ; Jiang, Bo ; Ma, Ning ; Tu, Shu-Jiang</creatorcontrib><description>A novel and efficient access to 2‐(argio(3‐methyl‐5‐oxo‐1‐phenyl‐4,5‐dihydro‐1H‐pyrazol‐4‐yl)methyl)‐3‐hydroxynaphthalene‐1,4‐dione derivatives from readily available substrates in neat water is described with aid of microwave irradiation. The results of our study provide a green, simple and practical one‐pot approach to the synthesis of 3‐hydroxynaphthalene‐1,4‐dione analogs in excellent yields without further purification.</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.798</identifier><language>eng</language><publisher>Hoboken, USA: Wiley Subscription Services, Inc., a Wiley company</publisher><ispartof>Journal of heterocyclic chemistry, 2012-05, Vol.49 (3), p.521-525</ispartof><rights>2012 HeteroCorporation</rights><rights>Copyright © 2012 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3318-b88a862243c1859e81e701139340b5cd040db416f219e720fc41d56c8f5fee473</citedby><cites>FETCH-LOGICAL-c3318-b88a862243c1859e81e701139340b5cd040db416f219e720fc41d56c8f5fee473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjhet.798$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjhet.798$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids></links><search><creatorcontrib>Wang, Shu-Liang</creatorcontrib><creatorcontrib>Ding, Jie</creatorcontrib><creatorcontrib>Shi, Fen</creatorcontrib><creatorcontrib>Liu, Yin-Ping</creatorcontrib><creatorcontrib>Jiang, Bo</creatorcontrib><creatorcontrib>Ma, Ning</creatorcontrib><creatorcontrib>Tu, Shu-Jiang</creatorcontrib><title>Green Synthesis of 3-Hydroxynaphthalene-1,4-dione Derivatives via Microwave-Assisted Three-Component Reactions in Neat Water</title><title>Journal of heterocyclic chemistry</title><addtitle>J. Heterocyclic Chem</addtitle><description>A novel and efficient access to 2‐(argio(3‐methyl‐5‐oxo‐1‐phenyl‐4,5‐dihydro‐1H‐pyrazol‐4‐yl)methyl)‐3‐hydroxynaphthalene‐1,4‐dione derivatives from readily available substrates in neat water is described with aid of microwave irradiation. The results of our study provide a green, simple and practical one‐pot approach to the synthesis of 3‐hydroxynaphthalene‐1,4‐dione analogs in excellent yields without further purification.</description><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp1kFFLIzEQx8OhYK0HfoSALz4YzWyym91Hqdoq6h13PTx8CenuLJtad2sSqwt-eFMqgg8-DcP85jfMn5B94MfAeXIybzAcqyL_QQZQSMFSKMQWGcRRwiBN_u-QXe_nsQWh1IC8jR1iS__2bWjQW0-7mgo26SvXvfatWTahMQtskcGRZJXtWqRn6OzKBLtCT1fW0Btbuu7FrJCd-mgIWNFpE61s1D0u40Ib6B80ZYjLntqW3qIJ9M4EdHtkuzYLjz8_6pD8uzifjibs-tf4cnR6zUohIGezPDd5liRSlJCnBeaAigOIQkg-S8uKS17NJGR1AgWqhNelhCrNyrxOa0SpxJAcbLxL1z09ow963j27Np7UkCWKF4WM8iE53FDxHe8d1nrp7KNxvQau19nqdbY6ZhtRtkFf7AL7bzl9NTmffuHX8bx-8sY96EwJleq727H-rW4u7uH-Sp-Jd_3QirM</recordid><startdate>201205</startdate><enddate>201205</enddate><creator>Wang, Shu-Liang</creator><creator>Ding, Jie</creator><creator>Shi, Fen</creator><creator>Liu, Yin-Ping</creator><creator>Jiang, Bo</creator><creator>Ma, Ning</creator><creator>Tu, Shu-Jiang</creator><general>Wiley Subscription Services, Inc., a Wiley company</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201205</creationdate><title>Green Synthesis of 3-Hydroxynaphthalene-1,4-dione Derivatives via Microwave-Assisted Three-Component Reactions in Neat Water</title><author>Wang, Shu-Liang ; Ding, Jie ; Shi, Fen ; Liu, Yin-Ping ; Jiang, Bo ; Ma, Ning ; Tu, Shu-Jiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3318-b88a862243c1859e81e701139340b5cd040db416f219e720fc41d56c8f5fee473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Shu-Liang</creatorcontrib><creatorcontrib>Ding, Jie</creatorcontrib><creatorcontrib>Shi, Fen</creatorcontrib><creatorcontrib>Liu, Yin-Ping</creatorcontrib><creatorcontrib>Jiang, Bo</creatorcontrib><creatorcontrib>Ma, Ning</creatorcontrib><creatorcontrib>Tu, Shu-Jiang</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Shu-Liang</au><au>Ding, Jie</au><au>Shi, Fen</au><au>Liu, Yin-Ping</au><au>Jiang, Bo</au><au>Ma, Ning</au><au>Tu, Shu-Jiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Green Synthesis of 3-Hydroxynaphthalene-1,4-dione Derivatives via Microwave-Assisted Three-Component Reactions in Neat Water</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><addtitle>J. Heterocyclic Chem</addtitle><date>2012-05</date><risdate>2012</risdate><volume>49</volume><issue>3</issue><spage>521</spage><epage>525</epage><pages>521-525</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>A novel and efficient access to 2‐(argio(3‐methyl‐5‐oxo‐1‐phenyl‐4,5‐dihydro‐1H‐pyrazol‐4‐yl)methyl)‐3‐hydroxynaphthalene‐1,4‐dione derivatives from readily available substrates in neat water is described with aid of microwave irradiation. The results of our study provide a green, simple and practical one‐pot approach to the synthesis of 3‐hydroxynaphthalene‐1,4‐dione analogs in excellent yields without further purification.</abstract><cop>Hoboken, USA</cop><pub>Wiley Subscription Services, Inc., a Wiley company</pub><doi>10.1002/jhet.798</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-152X
ispartof Journal of heterocyclic chemistry, 2012-05, Vol.49 (3), p.521-525
issn 0022-152X
1943-5193
language eng
recordid cdi_proquest_journals_1627099424
source Wiley Online Library Journals Frontfile Complete
title Green Synthesis of 3-Hydroxynaphthalene-1,4-dione Derivatives via Microwave-Assisted Three-Component Reactions in Neat Water
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T13%3A43%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Green%20Synthesis%20of%203-Hydroxynaphthalene-1,4-dione%20Derivatives%20via%20Microwave-Assisted%20Three-Component%20Reactions%20in%20Neat%20Water&rft.jtitle=Journal%20of%20heterocyclic%20chemistry&rft.au=Wang,%20Shu-Liang&rft.date=2012-05&rft.volume=49&rft.issue=3&rft.spage=521&rft.epage=525&rft.pages=521-525&rft.issn=0022-152X&rft.eissn=1943-5193&rft_id=info:doi/10.1002/jhet.798&rft_dat=%3Cproquest_cross%3E3505548491%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1627099424&rft_id=info:pmid/&rfr_iscdi=true