Efficient and Convenient Synthesis of 1,8-Dioxodecahydroacridine Derivatives Using Cu-Doped ZnO Nanocrystalline Powder as a Catalyst under Solvent-Free Conditions

A simple and convenient one-step method for synthesis of acridines and their derivatives from condensation of aromatic aldehydes, cyclic diketones, and aryl amines using Cu-doped ZnO nanocrystalline powder as a catalyst is reported. The present protocol provides several advantages such as good yield...

Full description

Saved in:
Bibliographic Details
Published in:TheScientificWorld 2013-01, Vol.2013 (2013), p.1-9
Main Authors: Alinezhad, Heshmatollah, Mohseni Tavakkoli, Sahar
Format: Article
Language:English
Subjects:
Acridines - chemical synthesis
Acridines - chemistry
Aldehydes
Amines
Aromatic compounds
Catalysis
Catalysts
Chemistry
Copper
Derivatives
Diketones
Fluorine
Metal Nanoparticles - chemistry
Metal Nanoparticles - ultrastructure
Molecular Structure
Nanocrystals
Nanoparticles
Photocatalysis
Powder
Powders
Reaction time
Solvents
Synthesis
Zinc Oxide
Zinc oxides
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c533t-24090588f0c4cdbd8a25923aa78b52d501c1dc9ed0ce1266b57649298a9e2e513
cites cdi_FETCH-LOGICAL-c533t-24090588f0c4cdbd8a25923aa78b52d501c1dc9ed0ce1266b57649298a9e2e513
container_end_page 9
container_issue 2013
container_start_page 1
container_title TheScientificWorld
container_volume 2013
creator Alinezhad, Heshmatollah
Mohseni Tavakkoli, Sahar
description A simple and convenient one-step method for synthesis of acridines and their derivatives from condensation of aromatic aldehydes, cyclic diketones, and aryl amines using Cu-doped ZnO nanocrystalline powder as a catalyst is reported. The present protocol provides several advantages such as good yields, short reaction time, easy workup, and simplicity in operation.
doi_str_mv 10.1155/2013/575636
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_d6bb33166b0f4dd4916349a8a64c5940</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_d6bb33166b0f4dd4916349a8a64c5940</doaj_id><sourcerecordid>2175217468</sourcerecordid><originalsourceid>FETCH-LOGICAL-c533t-24090588f0c4cdbd8a25923aa78b52d501c1dc9ed0ce1266b57649298a9e2e513</originalsourceid><addsrcrecordid>eNqNkk1vEzEQhlcIREPhxB1Z4gYs9ed-XCqhpIVKFUUqlRAXa9aeTRxt7WBvUvJ3-KU4TanaGwfL8vjRMzPSWxSvGf3ImFJHnDJxpGpViepJMWFK1GUt5Y-nxYQLVZUVk_SgeJHSklLR1Ew9Lw645K1kgk6KPyd974xDPxLwlkyD36C_fV5u_bjA5BIJPWEfmnLmwu9g0cBia2MAE511HskMo9vA6DaYyFVyfk6m63IWVmjJT39BvoIPJm7TCMOww7-FG4uRQCJAppCr-Yus_a52GYbcfCxPI-JuEutGF3x6WTzrYUj46u4-LK5OT75Pv5TnF5_Ppp_OS6OEGEsuaUtV0_TUSGM72wBXLRcAddMpbhVlhlnToqUGGa-qTtWVbHnbQIscFROHxdneawMs9Sq6a4hbHcDp20KIcw1xdGZAbauuE4JlCe2ltbJllZAtNFBJo1pJs-t471qtu2u0Jq8VYXgkffzj3ULPw0aLRgjKZRa8vRPE8GuNadTLsI4-7685q1U-smoy9X5PmRhSitjfd2BU78Khd-HQ-3Bk-s3Doe7Zf2nIwLs9sHDewo37PxtmBHt4ADOupBB_AXfEzUA</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2175217468</pqid></control><display><type>article</type><title>Efficient and Convenient Synthesis of 1,8-Dioxodecahydroacridine Derivatives Using Cu-Doped ZnO Nanocrystalline Powder as a Catalyst under Solvent-Free Conditions</title><source>Wiley Online Library Open Access</source><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Alinezhad, Heshmatollah ; Mohseni Tavakkoli, Sahar</creator><contributor>Hadjiarapoglou, L. ; D'Accolti, L.</contributor><creatorcontrib>Alinezhad, Heshmatollah ; Mohseni Tavakkoli, Sahar ; Hadjiarapoglou, L. ; D'Accolti, L.</creatorcontrib><description>A simple and convenient one-step method for synthesis of acridines and their derivatives from condensation of aromatic aldehydes, cyclic diketones, and aryl amines using Cu-doped ZnO nanocrystalline powder as a catalyst is reported. The present protocol provides several advantages such as good yields, short reaction time, easy workup, and simplicity in operation.</description><identifier>ISSN: 2356-6140</identifier><identifier>EISSN: 1537-744X</identifier><identifier>DOI: 10.1155/2013/575636</identifier><identifier>PMID: 24294130</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Acridines - chemical synthesis ; Acridines - chemistry ; Aldehydes ; Amines ; Aromatic compounds ; Catalysis ; Catalysts ; Chemistry ; Copper ; Derivatives ; Diketones ; Fluorine ; Metal Nanoparticles - chemistry ; Metal Nanoparticles - ultrastructure ; Molecular Structure ; Nanocrystals ; Nanoparticles ; Photocatalysis ; Powder ; Powders ; Reaction time ; Solvents ; Synthesis ; Zinc Oxide ; Zinc oxides</subject><ispartof>TheScientificWorld, 2013-01, Vol.2013 (2013), p.1-9</ispartof><rights>Copyright © 2013 Heshmatollah Alinezhad and Sahar Mohseni Tavakkoli.</rights><rights>Copyright © 2013 Heshmatollah Alinezhad and Sahar Mohseni Tavakkoli. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2013 H. Alinezhad and S. Mohseni Tavakkoli. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-24090588f0c4cdbd8a25923aa78b52d501c1dc9ed0ce1266b57649298a9e2e513</citedby><cites>FETCH-LOGICAL-c533t-24090588f0c4cdbd8a25923aa78b52d501c1dc9ed0ce1266b57649298a9e2e513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2175217468/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2175217468?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,44566,53766,53768,75096</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24294130$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Hadjiarapoglou, L.</contributor><contributor>D'Accolti, L.</contributor><creatorcontrib>Alinezhad, Heshmatollah</creatorcontrib><creatorcontrib>Mohseni Tavakkoli, Sahar</creatorcontrib><title>Efficient and Convenient Synthesis of 1,8-Dioxodecahydroacridine Derivatives Using Cu-Doped ZnO Nanocrystalline Powder as a Catalyst under Solvent-Free Conditions</title><title>TheScientificWorld</title><addtitle>ScientificWorldJournal</addtitle><description>A simple and convenient one-step method for synthesis of acridines and their derivatives from condensation of aromatic aldehydes, cyclic diketones, and aryl amines using Cu-doped ZnO nanocrystalline powder as a catalyst is reported. The present protocol provides several advantages such as good yields, short reaction time, easy workup, and simplicity in operation.</description><subject>Acridines - chemical synthesis</subject><subject>Acridines - chemistry</subject><subject>Aldehydes</subject><subject>Amines</subject><subject>Aromatic compounds</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chemistry</subject><subject>Copper</subject><subject>Derivatives</subject><subject>Diketones</subject><subject>Fluorine</subject><subject>Metal Nanoparticles - chemistry</subject><subject>Metal Nanoparticles - ultrastructure</subject><subject>Molecular Structure</subject><subject>Nanocrystals</subject><subject>Nanoparticles</subject><subject>Photocatalysis</subject><subject>Powder</subject><subject>Powders</subject><subject>Reaction time</subject><subject>Solvents</subject><subject>Synthesis</subject><subject>Zinc Oxide</subject><subject>Zinc oxides</subject><issn>2356-6140</issn><issn>1537-744X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkk1vEzEQhlcIREPhxB1Z4gYs9ed-XCqhpIVKFUUqlRAXa9aeTRxt7WBvUvJ3-KU4TanaGwfL8vjRMzPSWxSvGf3ImFJHnDJxpGpViepJMWFK1GUt5Y-nxYQLVZUVk_SgeJHSklLR1Ew9Lw645K1kgk6KPyd974xDPxLwlkyD36C_fV5u_bjA5BIJPWEfmnLmwu9g0cBia2MAE511HskMo9vA6DaYyFVyfk6m63IWVmjJT39BvoIPJm7TCMOww7-FG4uRQCJAppCr-Yus_a52GYbcfCxPI-JuEutGF3x6WTzrYUj46u4-LK5OT75Pv5TnF5_Ppp_OS6OEGEsuaUtV0_TUSGM72wBXLRcAddMpbhVlhlnToqUGGa-qTtWVbHnbQIscFROHxdneawMs9Sq6a4hbHcDp20KIcw1xdGZAbauuE4JlCe2ltbJllZAtNFBJo1pJs-t471qtu2u0Jq8VYXgkffzj3ULPw0aLRgjKZRa8vRPE8GuNadTLsI4-7685q1U-smoy9X5PmRhSitjfd2BU78Khd-HQ-3Bk-s3Doe7Zf2nIwLs9sHDewo37PxtmBHt4ADOupBB_AXfEzUA</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Alinezhad, Heshmatollah</creator><creator>Mohseni Tavakkoli, Sahar</creator><general>Hindawi Publishing Corporation</general><general>Hindawi Limited</general><general>Wiley</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130101</creationdate><title>Efficient and Convenient Synthesis of 1,8-Dioxodecahydroacridine Derivatives Using Cu-Doped ZnO Nanocrystalline Powder as a Catalyst under Solvent-Free Conditions</title><author>Alinezhad, Heshmatollah ; Mohseni Tavakkoli, Sahar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c533t-24090588f0c4cdbd8a25923aa78b52d501c1dc9ed0ce1266b57649298a9e2e513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Acridines - chemical synthesis</topic><topic>Acridines - chemistry</topic><topic>Aldehydes</topic><topic>Amines</topic><topic>Aromatic compounds</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Chemistry</topic><topic>Copper</topic><topic>Derivatives</topic><topic>Diketones</topic><topic>Fluorine</topic><topic>Metal Nanoparticles - chemistry</topic><topic>Metal Nanoparticles - ultrastructure</topic><topic>Molecular Structure</topic><topic>Nanocrystals</topic><topic>Nanoparticles</topic><topic>Photocatalysis</topic><topic>Powder</topic><topic>Powders</topic><topic>Reaction time</topic><topic>Solvents</topic><topic>Synthesis</topic><topic>Zinc Oxide</topic><topic>Zinc oxides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alinezhad, Heshmatollah</creatorcontrib><creatorcontrib>Mohseni Tavakkoli, Sahar</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>Middle East &amp; Africa Database</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health &amp; Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health &amp; Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied &amp; Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>TestCollectionTL3OpenAccess</collection><jtitle>TheScientificWorld</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alinezhad, Heshmatollah</au><au>Mohseni Tavakkoli, Sahar</au><au>Hadjiarapoglou, L.</au><au>D'Accolti, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient and Convenient Synthesis of 1,8-Dioxodecahydroacridine Derivatives Using Cu-Doped ZnO Nanocrystalline Powder as a Catalyst under Solvent-Free Conditions</atitle><jtitle>TheScientificWorld</jtitle><addtitle>ScientificWorldJournal</addtitle><date>2013-01-01</date><risdate>2013</risdate><volume>2013</volume><issue>2013</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>2356-6140</issn><eissn>1537-744X</eissn><abstract>A simple and convenient one-step method for synthesis of acridines and their derivatives from condensation of aromatic aldehydes, cyclic diketones, and aryl amines using Cu-doped ZnO nanocrystalline powder as a catalyst is reported. The present protocol provides several advantages such as good yields, short reaction time, easy workup, and simplicity in operation.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>24294130</pmid><doi>10.1155/2013/575636</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2356-6140
ispartof TheScientificWorld, 2013-01, Vol.2013 (2013), p.1-9
issn 2356-6140
1537-744X
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_d6bb33166b0f4dd4916349a8a64c5940
source Wiley Online Library Open Access; Publicly Available Content Database; PubMed Central
subjects Acridines - chemical synthesis
Acridines - chemistry
Aldehydes
Amines
Aromatic compounds
Catalysis
Catalysts
Chemistry
Copper
Derivatives
Diketones
Fluorine
Metal Nanoparticles - chemistry
Metal Nanoparticles - ultrastructure
Molecular Structure
Nanocrystals
Nanoparticles
Photocatalysis
Powder
Powders
Reaction time
Solvents
Synthesis
Zinc Oxide
Zinc oxides
title Efficient and Convenient Synthesis of 1,8-Dioxodecahydroacridine Derivatives Using Cu-Doped ZnO Nanocrystalline Powder as a Catalyst under Solvent-Free Conditions
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-23T20%3A08%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Efficient%20and%20Convenient%20Synthesis%20of%201,8-Dioxodecahydroacridine%20Derivatives%20Using%20Cu-Doped%20ZnO%20Nanocrystalline%20Powder%20as%20a%20Catalyst%20under%20Solvent-Free%20Conditions&rft.jtitle=TheScientificWorld&rft.au=Alinezhad,%20Heshmatollah&rft.date=2013-01-01&rft.volume=2013&rft.issue=2013&rft.spage=1&rft.epage=9&rft.pages=1-9&rft.issn=2356-6140&rft.eissn=1537-744X&rft_id=info:doi/10.1155/2013/575636&rft_dat=%3Cproquest_doaj_%3E2175217468%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c533t-24090588f0c4cdbd8a25923aa78b52d501c1dc9ed0ce1266b57649298a9e2e513%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2175217468&rft_id=info:pmid/24294130&rfr_iscdi=true