Microwave‐Assisted Ruthenium(II)‐Catalyzed C−H/N−O Activation of N‐Methoxybenzamides with Alkynylsulfane

An annulation of phenyl(phenylethynyl)sulfane and N‐methoxybenzamides through ruthenium C−H/N−O activation is reported. A wide variety of 4‐aryl‐3‐(aryl/alkylthio)isoquinolin‐1(2H)‐one derivatives are obtained in moderate to good yields. Microwave dinner: An annulation of phenyl(phenylethynyl)sulfan...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Asian journal of organic chemistry 2019-10, Vol.8 (10), p.1830-1833
Hauptverfasser: Sarathkumar, Sundaramoorthi, Kavala, Veerababurao, Yao, Ching‐Fa
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1833
container_issue 10
container_start_page 1830
container_title Asian journal of organic chemistry
container_volume 8
creator Sarathkumar, Sundaramoorthi
Kavala, Veerababurao
Yao, Ching‐Fa
description An annulation of phenyl(phenylethynyl)sulfane and N‐methoxybenzamides through ruthenium C−H/N−O activation is reported. A wide variety of 4‐aryl‐3‐(aryl/alkylthio)isoquinolin‐1(2H)‐one derivatives are obtained in moderate to good yields. Microwave dinner: An annulation of phenyl(phenylethynyl)sulfane and N‐methoxybenzamide through ruthenium C−H/N−O activation is reported herein.
doi_str_mv 10.1002/ajoc.201900383
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2303053061</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2303053061</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3173-1a0661ede1f62f909a9cdfb9ed861f65daf1a3e9643faa69110cdf3b26f1fff63</originalsourceid><addsrcrecordid>eNqFkD9PwzAQxS0EElXpyhyJBYa0vpg49RhFQIv6R0IwW25iqy5pUmKnJZ0YGREfsZ8EV0Vl5IY7697vnaWH0CXgLmAc9MSiTLsBBoYx6ZMT1AqAET_sQ3h6fOPoHHWMWWBXUcQgYC1UjXValRuxlruPr9gYbazMvKfazmWh6-X1cHjjhERYkTdbpyS7z-9Bb-L61ItTq9fC6rLwSuVNHDeWdl6-NzNZbMVSZ9J4G23nXpy_NkWTmzpXopAX6EyJ3MjO72yjl_u752Tgj6YPwyQe-SmBiPggMKUgMwmKBophJliaqRmTWZ-6VZgJBYJIRm-JEoIyAOx0MguoAqUUJW10dbi7qsq3WhrLF2VdFe5LHhBMcEgwBUd1D5SLwZhKKr6q9FJUDQfM99HyfbT8GK0zsINho3PZ_EPz-HGa_Hl_ALlsg8A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2303053061</pqid></control><display><type>article</type><title>Microwave‐Assisted Ruthenium(II)‐Catalyzed C−H/N−O Activation of N‐Methoxybenzamides with Alkynylsulfane</title><source>Wiley Online Library All Journals</source><creator>Sarathkumar, Sundaramoorthi ; Kavala, Veerababurao ; Yao, Ching‐Fa</creator><creatorcontrib>Sarathkumar, Sundaramoorthi ; Kavala, Veerababurao ; Yao, Ching‐Fa</creatorcontrib><description>An annulation of phenyl(phenylethynyl)sulfane and N‐methoxybenzamides through ruthenium C−H/N−O activation is reported. A wide variety of 4‐aryl‐3‐(aryl/alkylthio)isoquinolin‐1(2H)‐one derivatives are obtained in moderate to good yields. Microwave dinner: An annulation of phenyl(phenylethynyl)sulfane and N‐methoxybenzamide through ruthenium C−H/N−O activation is reported herein.</description><identifier>ISSN: 2193-5807</identifier><identifier>EISSN: 2193-5815</identifier><identifier>DOI: 10.1002/ajoc.201900383</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>4-aryl-3-(aryl/alkylthio)isoquinolin-1(2H)-ones ; Activation ; alkynylsulfanes ; Aromatic compounds ; Chemical reactions ; C−H activation ; microwave chemistry ; Organic chemistry ; Ruthenium ; Ruthenium compounds</subject><ispartof>Asian journal of organic chemistry, 2019-10, Vol.8 (10), p.1830-1833</ispartof><rights>2019 Wiley‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3173-1a0661ede1f62f909a9cdfb9ed861f65daf1a3e9643faa69110cdf3b26f1fff63</citedby><cites>FETCH-LOGICAL-c3173-1a0661ede1f62f909a9cdfb9ed861f65daf1a3e9643faa69110cdf3b26f1fff63</cites><orcidid>0000-0002-8692-5156</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fajoc.201900383$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fajoc.201900383$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Sarathkumar, Sundaramoorthi</creatorcontrib><creatorcontrib>Kavala, Veerababurao</creatorcontrib><creatorcontrib>Yao, Ching‐Fa</creatorcontrib><title>Microwave‐Assisted Ruthenium(II)‐Catalyzed C−H/N−O Activation of N‐Methoxybenzamides with Alkynylsulfane</title><title>Asian journal of organic chemistry</title><description>An annulation of phenyl(phenylethynyl)sulfane and N‐methoxybenzamides through ruthenium C−H/N−O activation is reported. A wide variety of 4‐aryl‐3‐(aryl/alkylthio)isoquinolin‐1(2H)‐one derivatives are obtained in moderate to good yields. Microwave dinner: An annulation of phenyl(phenylethynyl)sulfane and N‐methoxybenzamide through ruthenium C−H/N−O activation is reported herein.</description><subject>4-aryl-3-(aryl/alkylthio)isoquinolin-1(2H)-ones</subject><subject>Activation</subject><subject>alkynylsulfanes</subject><subject>Aromatic compounds</subject><subject>Chemical reactions</subject><subject>C−H activation</subject><subject>microwave chemistry</subject><subject>Organic chemistry</subject><subject>Ruthenium</subject><subject>Ruthenium compounds</subject><issn>2193-5807</issn><issn>2193-5815</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkD9PwzAQxS0EElXpyhyJBYa0vpg49RhFQIv6R0IwW25iqy5pUmKnJZ0YGREfsZ8EV0Vl5IY7697vnaWH0CXgLmAc9MSiTLsBBoYx6ZMT1AqAET_sQ3h6fOPoHHWMWWBXUcQgYC1UjXValRuxlruPr9gYbazMvKfazmWh6-X1cHjjhERYkTdbpyS7z-9Bb-L61ItTq9fC6rLwSuVNHDeWdl6-NzNZbMVSZ9J4G23nXpy_NkWTmzpXopAX6EyJ3MjO72yjl_u752Tgj6YPwyQe-SmBiPggMKUgMwmKBophJliaqRmTWZ-6VZgJBYJIRm-JEoIyAOx0MguoAqUUJW10dbi7qsq3WhrLF2VdFe5LHhBMcEgwBUd1D5SLwZhKKr6q9FJUDQfM99HyfbT8GK0zsINho3PZ_EPz-HGa_Hl_ALlsg8A</recordid><startdate>201910</startdate><enddate>201910</enddate><creator>Sarathkumar, Sundaramoorthi</creator><creator>Kavala, Veerababurao</creator><creator>Yao, Ching‐Fa</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-8692-5156</orcidid></search><sort><creationdate>201910</creationdate><title>Microwave‐Assisted Ruthenium(II)‐Catalyzed C−H/N−O Activation of N‐Methoxybenzamides with Alkynylsulfane</title><author>Sarathkumar, Sundaramoorthi ; Kavala, Veerababurao ; Yao, Ching‐Fa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3173-1a0661ede1f62f909a9cdfb9ed861f65daf1a3e9643faa69110cdf3b26f1fff63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>4-aryl-3-(aryl/alkylthio)isoquinolin-1(2H)-ones</topic><topic>Activation</topic><topic>alkynylsulfanes</topic><topic>Aromatic compounds</topic><topic>Chemical reactions</topic><topic>C−H activation</topic><topic>microwave chemistry</topic><topic>Organic chemistry</topic><topic>Ruthenium</topic><topic>Ruthenium compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sarathkumar, Sundaramoorthi</creatorcontrib><creatorcontrib>Kavala, Veerababurao</creatorcontrib><creatorcontrib>Yao, Ching‐Fa</creatorcontrib><collection>CrossRef</collection><jtitle>Asian journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sarathkumar, Sundaramoorthi</au><au>Kavala, Veerababurao</au><au>Yao, Ching‐Fa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microwave‐Assisted Ruthenium(II)‐Catalyzed C−H/N−O Activation of N‐Methoxybenzamides with Alkynylsulfane</atitle><jtitle>Asian journal of organic chemistry</jtitle><date>2019-10</date><risdate>2019</risdate><volume>8</volume><issue>10</issue><spage>1830</spage><epage>1833</epage><pages>1830-1833</pages><issn>2193-5807</issn><eissn>2193-5815</eissn><abstract>An annulation of phenyl(phenylethynyl)sulfane and N‐methoxybenzamides through ruthenium C−H/N−O activation is reported. A wide variety of 4‐aryl‐3‐(aryl/alkylthio)isoquinolin‐1(2H)‐one derivatives are obtained in moderate to good yields. Microwave dinner: An annulation of phenyl(phenylethynyl)sulfane and N‐methoxybenzamide through ruthenium C−H/N−O activation is reported herein.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ajoc.201900383</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-8692-5156</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 2193-5807
ispartof Asian journal of organic chemistry, 2019-10, Vol.8 (10), p.1830-1833
issn 2193-5807
2193-5815
language eng
recordid cdi_proquest_journals_2303053061
source Wiley Online Library All Journals
subjects 4-aryl-3-(aryl/alkylthio)isoquinolin-1(2H)-ones
Activation
alkynylsulfanes
Aromatic compounds
Chemical reactions
C−H activation
microwave chemistry
Organic chemistry
Ruthenium
Ruthenium compounds
title Microwave‐Assisted Ruthenium(II)‐Catalyzed C−H/N−O Activation of N‐Methoxybenzamides with Alkynylsulfane
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T06%3A04%3A22IST&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=Microwave%E2%80%90Assisted%20Ruthenium(II)%E2%80%90Catalyzed%20C%E2%88%92H/N%E2%88%92O%20Activation%20of%20N%E2%80%90Methoxybenzamides%20with%20Alkynylsulfane&rft.jtitle=Asian%20journal%20of%20organic%20chemistry&rft.au=Sarathkumar,%20Sundaramoorthi&rft.date=2019-10&rft.volume=8&rft.issue=10&rft.spage=1830&rft.epage=1833&rft.pages=1830-1833&rft.issn=2193-5807&rft.eissn=2193-5815&rft_id=info:doi/10.1002/ajoc.201900383&rft_dat=%3Cproquest_cross%3E2303053061%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=2303053061&rft_id=info:pmid/&rfr_iscdi=true