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Palladium‐Catalyzed Mizoroki–Heck‐Type Alkenylation of Monoaryldialkylsulfoniums
Mizoroki–Heck‐type alkenylation of monoaryldialkylsulfoniums has been accomplished by means of palladium catalysts. Various combinations of monoarylsulfoniums and alkenes were adapted to the present reaction. Because monoaryldimethylsulfoniums were readily prepared from the corresponding aryl methyl...
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Published in: | Chemistry, an Asian journal an Asian journal, 2018-09, Vol.13 (17), p.2397-2400 |
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container_end_page | 2400 |
container_issue | 17 |
container_start_page | 2397 |
container_title | Chemistry, an Asian journal |
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creator | Uno, Daisuke Minami, Hiroko Otsuka, Shinya Nogi, Keisuke Yorimitsu, Hideki |
description | Mizoroki–Heck‐type alkenylation of monoaryldialkylsulfoniums has been accomplished by means of palladium catalysts. Various combinations of monoarylsulfoniums and alkenes were adapted to the present reaction. Because monoaryldimethylsulfoniums were readily prepared from the corresponding aryl methyl sulfides and methyl triflate, one‐pot alkenylation of aryl methyl sulfide could also be executed.
Mizoroki–Heck‐type alkenylation of monoaryldialkylsulfoniums has been accomplished by means of palladium catalysts. Because monoaryldimethylsulfoniums were readily prepared from the corresponding aryl methyl sulfides and methyl triflate, one‐pot alkenylation of aryl methyl sulfide could also be executed. |
doi_str_mv | 10.1002/asia.201800489 |
format | article |
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Mizoroki–Heck‐type alkenylation of monoaryldialkylsulfoniums has been accomplished by means of palladium catalysts. Because monoaryldimethylsulfoniums were readily prepared from the corresponding aryl methyl sulfides and methyl triflate, one‐pot alkenylation of aryl methyl sulfide could also be executed.</description><identifier>ISSN: 1861-4728</identifier><identifier>EISSN: 1861-471X</identifier><identifier>DOI: 10.1002/asia.201800489</identifier><identifier>PMID: 29729085</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Alkenes ; alkenylation ; Aromatic compounds ; aryl methyl sulfide ; arylsulfonium ; Chemistry ; Palladium</subject><ispartof>Chemistry, an Asian journal, 2018-09, Vol.13 (17), p.2397-2400</ispartof><rights>2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4769-63637501a86d45ad1bf61db7044190de62288ce46f17f14f6395fc5f4fd33ec23</citedby><cites>FETCH-LOGICAL-c4769-63637501a86d45ad1bf61db7044190de62288ce46f17f14f6395fc5f4fd33ec23</cites><orcidid>0000-0002-0153-1888 ; 0000-0001-8478-1227 ; 0000-0001-5598-9707</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29729085$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uno, Daisuke</creatorcontrib><creatorcontrib>Minami, Hiroko</creatorcontrib><creatorcontrib>Otsuka, Shinya</creatorcontrib><creatorcontrib>Nogi, Keisuke</creatorcontrib><creatorcontrib>Yorimitsu, Hideki</creatorcontrib><title>Palladium‐Catalyzed Mizoroki–Heck‐Type Alkenylation of Monoaryldialkylsulfoniums</title><title>Chemistry, an Asian journal</title><addtitle>Chem Asian J</addtitle><description>Mizoroki–Heck‐type alkenylation of monoaryldialkylsulfoniums has been accomplished by means of palladium catalysts. Various combinations of monoarylsulfoniums and alkenes were adapted to the present reaction. Because monoaryldimethylsulfoniums were readily prepared from the corresponding aryl methyl sulfides and methyl triflate, one‐pot alkenylation of aryl methyl sulfide could also be executed.
Mizoroki–Heck‐type alkenylation of monoaryldialkylsulfoniums has been accomplished by means of palladium catalysts. Because monoaryldimethylsulfoniums were readily prepared from the corresponding aryl methyl sulfides and methyl triflate, one‐pot alkenylation of aryl methyl sulfide could also be executed.</description><subject>Alkenes</subject><subject>alkenylation</subject><subject>Aromatic compounds</subject><subject>aryl methyl sulfide</subject><subject>arylsulfonium</subject><subject>Chemistry</subject><subject>Palladium</subject><issn>1861-4728</issn><issn>1861-471X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkMtKAzEUQIMotj62LqXgxs3UJJPJJMtSfIFFwQfuQjpJIE5mUicdZFz5CYJ_2C8xpbWCG1cJ5NxD7gHgCMEhghCfyWDlEEPEICSMb4E-YhQlJEfP25s7Zj2wF8ILhBmGnO2CHuY55pBlffB0J52TyrbV4uNzLOfSde9aDSb23Te-tIuPrytdlPHtoZvpwciVuu6cnFtfD7wZTHztZdM5ZaUrOxdaZ3wdXeEA7Bjpgj5cn_vg8eL8YXyV3NxeXo9HN0lBcsoTmtI0zyCSjCqSSYWmhiI1zSEhiEOlKcaMFZpQg3KDiKEpz0yRGWJUmuoCp_vgdOWdNf611WEuKhsKHVeqtW-DwDDNMMEwZxE9-YO--Lap4-_EsgpnJGMkUsMVVTQ-hEYbMWtsFXcUCIplcbEsLjbF48DxWttOK602-E_iCPAV8Gad7v7RidH99ehX_g2PxJCG</recordid><startdate>20180904</startdate><enddate>20180904</enddate><creator>Uno, Daisuke</creator><creator>Minami, Hiroko</creator><creator>Otsuka, Shinya</creator><creator>Nogi, Keisuke</creator><creator>Yorimitsu, Hideki</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0153-1888</orcidid><orcidid>https://orcid.org/0000-0001-8478-1227</orcidid><orcidid>https://orcid.org/0000-0001-5598-9707</orcidid></search><sort><creationdate>20180904</creationdate><title>Palladium‐Catalyzed Mizoroki–Heck‐Type Alkenylation of Monoaryldialkylsulfoniums</title><author>Uno, Daisuke ; Minami, Hiroko ; Otsuka, Shinya ; Nogi, Keisuke ; Yorimitsu, Hideki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4769-63637501a86d45ad1bf61db7044190de62288ce46f17f14f6395fc5f4fd33ec23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Alkenes</topic><topic>alkenylation</topic><topic>Aromatic compounds</topic><topic>aryl methyl sulfide</topic><topic>arylsulfonium</topic><topic>Chemistry</topic><topic>Palladium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uno, Daisuke</creatorcontrib><creatorcontrib>Minami, Hiroko</creatorcontrib><creatorcontrib>Otsuka, Shinya</creatorcontrib><creatorcontrib>Nogi, Keisuke</creatorcontrib><creatorcontrib>Yorimitsu, Hideki</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry, an Asian journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uno, Daisuke</au><au>Minami, Hiroko</au><au>Otsuka, Shinya</au><au>Nogi, Keisuke</au><au>Yorimitsu, Hideki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Palladium‐Catalyzed Mizoroki–Heck‐Type Alkenylation of Monoaryldialkylsulfoniums</atitle><jtitle>Chemistry, an Asian journal</jtitle><addtitle>Chem Asian J</addtitle><date>2018-09-04</date><risdate>2018</risdate><volume>13</volume><issue>17</issue><spage>2397</spage><epage>2400</epage><pages>2397-2400</pages><issn>1861-4728</issn><eissn>1861-471X</eissn><abstract>Mizoroki–Heck‐type alkenylation of monoaryldialkylsulfoniums has been accomplished by means of palladium catalysts. Various combinations of monoarylsulfoniums and alkenes were adapted to the present reaction. Because monoaryldimethylsulfoniums were readily prepared from the corresponding aryl methyl sulfides and methyl triflate, one‐pot alkenylation of aryl methyl sulfide could also be executed.
Mizoroki–Heck‐type alkenylation of monoaryldialkylsulfoniums has been accomplished by means of palladium catalysts. Because monoaryldimethylsulfoniums were readily prepared from the corresponding aryl methyl sulfides and methyl triflate, one‐pot alkenylation of aryl methyl sulfide could also be executed.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29729085</pmid><doi>10.1002/asia.201800489</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-0153-1888</orcidid><orcidid>https://orcid.org/0000-0001-8478-1227</orcidid><orcidid>https://orcid.org/0000-0001-5598-9707</orcidid></addata></record> |
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issn | 1861-4728 1861-471X |
language | eng |
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source | Wiley |
subjects | Alkenes alkenylation Aromatic compounds aryl methyl sulfide arylsulfonium Chemistry Palladium |
title | Palladium‐Catalyzed Mizoroki–Heck‐Type Alkenylation of Monoaryldialkylsulfoniums |
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