Convenient and Efficient Method for the Synthesis of N-Heteroaryl Aminonaphthols under Solvent-Free Conditions
A convenient, efficient and green synthesis of N‐heteroaryl aminonaphthols has been developed by one‐pot, three‐component condensation of β‐naphthol, heteroaryl amines and substituted benzaldehydes under solvent‐free conditions at elevated temperature. The advantages of these reactions are simplicit...
Gespeichert in:
| Veröffentlicht in: | Chinese journal of chemistry 2010-05, Vol.28 (5), p.825-832 |
|---|---|
| Hauptverfasser: | , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 832 |
|---|---|
| container_issue | 5 |
| container_start_page | 825 |
| container_title | Chinese journal of chemistry |
| container_volume | 28 |
| creator | Olyaei, Abolfazl Raoufmoghaddam, Saeed Sadeghpour, Mahdieh Ebadzadeh, Behruz |
| description | A convenient, efficient and green synthesis of N‐heteroaryl aminonaphthols has been developed by one‐pot, three‐component condensation of β‐naphthol, heteroaryl amines and substituted benzaldehydes under solvent‐free conditions at elevated temperature. The advantages of these reactions are simplicity of the reaction procedure, short reaction times, simple work‐up, catalyst‐free conditions and pure products in good to excellent yields.
A convenient, efficient and green synthesis of N‐heteroaryl aminonaphthols has been developed by one‐pot, three‐component condensation of β‐naphthol, heteroaryl amines and substituted benzaldehydes under solvent‐free conditions at elevated temperature. The advantages of these reactions are simplicity of the reaction procedure, short reaction times, simple work‐up, catalyst‐free conditions and pure products in good to excellent yields. |
| doi_str_mv | 10.1002/cjoc.201090153 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1766804726</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3957957041</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3953-675f8edacca68409926a4221bf42ca0e9710329235c1299481fb7951e94c662d3</originalsourceid><addsrcrecordid>eNqFkD1PwzAQhiMEEuVjZbbEnGI7iV2PVVQIiMJQEN0s45xVl9Qudgr032MoQmxMdyc9z53uzbIzgocEY3qhl14PKSZYYFIVe9mAMFLmHLNqP_UYk5zhcn6YHcW4TDznlA0yV3v3Bs6C65FyLZoYY_X3NIV-4VtkfED9AtBs61KJNiJv0F3eQA_Bq7Dt0HhlnXdqvUh8F9HGtRDQzHdpbZ9fBgCUbrS2t97Fk-zAqC7C6U89zh4vJw91k9_eX13X49tcF6IqcsYrM4JWaa3YqMRCUKZKSsmzKalWGAQnuKCCFpUmVIhyRMwzFxUBUWrGaFscZ-e7vevgXzcQe7n0m-DSSUk4YyNcpu8TNdxROvgYAxi5DnaVnpIEy69M5Vem8jfTJIid8G472P5Dy_rmvv7r5jvXxh4-fl0VXiTjBa_k092V5E09b-bNVNLiExfuil4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1766804726</pqid></control><display><type>article</type><title>Convenient and Efficient Method for the Synthesis of N-Heteroaryl Aminonaphthols under Solvent-Free Conditions</title><source>Wiley Online Library All Journals</source><creator>Olyaei, Abolfazl ; Raoufmoghaddam, Saeed ; Sadeghpour, Mahdieh ; Ebadzadeh, Behruz</creator><creatorcontrib>Olyaei, Abolfazl ; Raoufmoghaddam, Saeed ; Sadeghpour, Mahdieh ; Ebadzadeh, Behruz</creatorcontrib><description>A convenient, efficient and green synthesis of N‐heteroaryl aminonaphthols has been developed by one‐pot, three‐component condensation of β‐naphthol, heteroaryl amines and substituted benzaldehydes under solvent‐free conditions at elevated temperature. The advantages of these reactions are simplicity of the reaction procedure, short reaction times, simple work‐up, catalyst‐free conditions and pure products in good to excellent yields.
A convenient, efficient and green synthesis of N‐heteroaryl aminonaphthols has been developed by one‐pot, three‐component condensation of β‐naphthol, heteroaryl amines and substituted benzaldehydes under solvent‐free conditions at elevated temperature. The advantages of these reactions are simplicity of the reaction procedure, short reaction times, simple work‐up, catalyst‐free conditions and pure products in good to excellent yields.</description><identifier>ISSN: 1001-604X</identifier><identifier>EISSN: 1614-7065</identifier><identifier>DOI: 10.1002/cjoc.201090153</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>aminonaphthol ; Betti base ; heteroaryl amine ; solvent-free ; β-naphthol</subject><ispartof>Chinese journal of chemistry, 2010-05, Vol.28 (5), p.825-832</ispartof><rights>Copyright © 2010 SIOC, CAS, Shanghai & WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2010 SIOC, CAS, Shanghai & WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3953-675f8edacca68409926a4221bf42ca0e9710329235c1299481fb7951e94c662d3</citedby><cites>FETCH-LOGICAL-c3953-675f8edacca68409926a4221bf42ca0e9710329235c1299481fb7951e94c662d3</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%2Fcjoc.201090153$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcjoc.201090153$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Olyaei, Abolfazl</creatorcontrib><creatorcontrib>Raoufmoghaddam, Saeed</creatorcontrib><creatorcontrib>Sadeghpour, Mahdieh</creatorcontrib><creatorcontrib>Ebadzadeh, Behruz</creatorcontrib><title>Convenient and Efficient Method for the Synthesis of N-Heteroaryl Aminonaphthols under Solvent-Free Conditions</title><title>Chinese journal of chemistry</title><addtitle>Chin. J. Chem</addtitle><description>A convenient, efficient and green synthesis of N‐heteroaryl aminonaphthols has been developed by one‐pot, three‐component condensation of β‐naphthol, heteroaryl amines and substituted benzaldehydes under solvent‐free conditions at elevated temperature. The advantages of these reactions are simplicity of the reaction procedure, short reaction times, simple work‐up, catalyst‐free conditions and pure products in good to excellent yields.
A convenient, efficient and green synthesis of N‐heteroaryl aminonaphthols has been developed by one‐pot, three‐component condensation of β‐naphthol, heteroaryl amines and substituted benzaldehydes under solvent‐free conditions at elevated temperature. The advantages of these reactions are simplicity of the reaction procedure, short reaction times, simple work‐up, catalyst‐free conditions and pure products in good to excellent yields.</description><subject>aminonaphthol</subject><subject>Betti base</subject><subject>heteroaryl amine</subject><subject>solvent-free</subject><subject>β-naphthol</subject><issn>1001-604X</issn><issn>1614-7065</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkD1PwzAQhiMEEuVjZbbEnGI7iV2PVVQIiMJQEN0s45xVl9Qudgr032MoQmxMdyc9z53uzbIzgocEY3qhl14PKSZYYFIVe9mAMFLmHLNqP_UYk5zhcn6YHcW4TDznlA0yV3v3Bs6C65FyLZoYY_X3NIV-4VtkfED9AtBs61KJNiJv0F3eQA_Bq7Dt0HhlnXdqvUh8F9HGtRDQzHdpbZ9fBgCUbrS2t97Fk-zAqC7C6U89zh4vJw91k9_eX13X49tcF6IqcsYrM4JWaa3YqMRCUKZKSsmzKalWGAQnuKCCFpUmVIhyRMwzFxUBUWrGaFscZ-e7vevgXzcQe7n0m-DSSUk4YyNcpu8TNdxROvgYAxi5DnaVnpIEy69M5Vem8jfTJIid8G472P5Dy_rmvv7r5jvXxh4-fl0VXiTjBa_k092V5E09b-bNVNLiExfuil4</recordid><startdate>201005</startdate><enddate>201005</enddate><creator>Olyaei, Abolfazl</creator><creator>Raoufmoghaddam, Saeed</creator><creator>Sadeghpour, Mahdieh</creator><creator>Ebadzadeh, Behruz</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201005</creationdate><title>Convenient and Efficient Method for the Synthesis of N-Heteroaryl Aminonaphthols under Solvent-Free Conditions</title><author>Olyaei, Abolfazl ; Raoufmoghaddam, Saeed ; Sadeghpour, Mahdieh ; Ebadzadeh, Behruz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3953-675f8edacca68409926a4221bf42ca0e9710329235c1299481fb7951e94c662d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>aminonaphthol</topic><topic>Betti base</topic><topic>heteroaryl amine</topic><topic>solvent-free</topic><topic>β-naphthol</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Olyaei, Abolfazl</creatorcontrib><creatorcontrib>Raoufmoghaddam, Saeed</creatorcontrib><creatorcontrib>Sadeghpour, Mahdieh</creatorcontrib><creatorcontrib>Ebadzadeh, Behruz</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Chinese journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Olyaei, Abolfazl</au><au>Raoufmoghaddam, Saeed</au><au>Sadeghpour, Mahdieh</au><au>Ebadzadeh, Behruz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Convenient and Efficient Method for the Synthesis of N-Heteroaryl Aminonaphthols under Solvent-Free Conditions</atitle><jtitle>Chinese journal of chemistry</jtitle><addtitle>Chin. J. Chem</addtitle><date>2010-05</date><risdate>2010</risdate><volume>28</volume><issue>5</issue><spage>825</spage><epage>832</epage><pages>825-832</pages><issn>1001-604X</issn><eissn>1614-7065</eissn><abstract>A convenient, efficient and green synthesis of N‐heteroaryl aminonaphthols has been developed by one‐pot, three‐component condensation of β‐naphthol, heteroaryl amines and substituted benzaldehydes under solvent‐free conditions at elevated temperature. The advantages of these reactions are simplicity of the reaction procedure, short reaction times, simple work‐up, catalyst‐free conditions and pure products in good to excellent yields.
A convenient, efficient and green synthesis of N‐heteroaryl aminonaphthols has been developed by one‐pot, three‐component condensation of β‐naphthol, heteroaryl amines and substituted benzaldehydes under solvent‐free conditions at elevated temperature. The advantages of these reactions are simplicity of the reaction procedure, short reaction times, simple work‐up, catalyst‐free conditions and pure products in good to excellent yields.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/cjoc.201090153</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1001-604X |
| ispartof | Chinese journal of chemistry, 2010-05, Vol.28 (5), p.825-832 |
| issn | 1001-604X 1614-7065 |
| language | eng |
| recordid | cdi_proquest_journals_1766804726 |
| source | Wiley Online Library All Journals |
| subjects | aminonaphthol Betti base heteroaryl amine solvent-free β-naphthol |
| title | Convenient and Efficient Method for the Synthesis of N-Heteroaryl Aminonaphthols under Solvent-Free Conditions |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T00%3A16%3A58IST&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=Convenient%20and%20Efficient%20Method%20for%20the%20Synthesis%20of%20N-Heteroaryl%20Aminonaphthols%20under%20Solvent-Free%20Conditions&rft.jtitle=Chinese%20journal%20of%20chemistry&rft.au=Olyaei,%20Abolfazl&rft.date=2010-05&rft.volume=28&rft.issue=5&rft.spage=825&rft.epage=832&rft.pages=825-832&rft.issn=1001-604X&rft.eissn=1614-7065&rft_id=info:doi/10.1002/cjoc.201090153&rft_dat=%3Cproquest_cross%3E3957957041%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=1766804726&rft_id=info:pmid/&rfr_iscdi=true |