Bifunctional two-carbon reagent made from acetylene via 1,2-difunctionalization and its applications
There are very limited approaches to directly gluing two molecules for the production of internal alkenes using the vastly abundant acetylene via 1,2-difunctionalization. Conversion of gaseous acetylene to internal alkenes via 1,2-difunctionalization in a desired manner is not as easy as it might be...
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Veröffentlicht in: | Science China. Chemistry 2024-03, Vol.67 (3), p.936-944 |
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creator | Yang, Bo Li, Kangkui Wang, Yongdong Zhu, Shifa |
description | There are very limited approaches to directly gluing two molecules for the production of internal alkenes using the vastly abundant acetylene
via
1,2-difunctionalization. Conversion of gaseous acetylene to internal alkenes
via
1,2-difunctionalization in a desired manner is not as easy as it might be expected due to the potential competition reactions between acetylene and alkene produced and the difficulty in handling this harmful reagent and controlling the regio- and stereoselectivity. In this work, we designed an efficient catalytic system for the incorporation of acetylene gas into tremendous (
E
)-
β
-bromo vinylsulfones, which are bench-stable, easy to operate, and can function as bifunctional acetylene and show a rich reactivity profile in Sonogashira coupling, Heck coupling, substituted reaction, and various desulfonylation transformations, providing numerous internal alkenes. |
doi_str_mv | 10.1007/s11426-023-1871-y |
format | Article |
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via
1,2-difunctionalization. Conversion of gaseous acetylene to internal alkenes
via
1,2-difunctionalization in a desired manner is not as easy as it might be expected due to the potential competition reactions between acetylene and alkene produced and the difficulty in handling this harmful reagent and controlling the regio- and stereoselectivity. In this work, we designed an efficient catalytic system for the incorporation of acetylene gas into tremendous (
E
)-
β
-bromo vinylsulfones, which are bench-stable, easy to operate, and can function as bifunctional acetylene and show a rich reactivity profile in Sonogashira coupling, Heck coupling, substituted reaction, and various desulfonylation transformations, providing numerous internal alkenes.</description><identifier>ISSN: 1674-7291</identifier><identifier>EISSN: 1869-1870</identifier><identifier>DOI: 10.1007/s11426-023-1871-y</identifier><language>eng</language><publisher>Beijing: Science China Press</publisher><subject>Acetylene ; Alkenes ; Carbon ; Chemical engineering ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Coupling ; Laboratories ; Reagents ; Stereoselectivity</subject><ispartof>Science China. Chemistry, 2024-03, Vol.67 (3), p.936-944</ispartof><rights>Science China Press 2024</rights><rights>Science China Press 2024.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-a7e86a78d05795ce279070f4b7e4e935f94c93f5857e482072f362f527c8d133</citedby><cites>FETCH-LOGICAL-c316t-a7e86a78d05795ce279070f4b7e4e935f94c93f5857e482072f362f527c8d133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11426-023-1871-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11426-023-1871-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids></links><search><creatorcontrib>Yang, Bo</creatorcontrib><creatorcontrib>Li, Kangkui</creatorcontrib><creatorcontrib>Wang, Yongdong</creatorcontrib><creatorcontrib>Zhu, Shifa</creatorcontrib><title>Bifunctional two-carbon reagent made from acetylene via 1,2-difunctionalization and its applications</title><title>Science China. Chemistry</title><addtitle>Sci. China Chem</addtitle><description>There are very limited approaches to directly gluing two molecules for the production of internal alkenes using the vastly abundant acetylene
via
1,2-difunctionalization. Conversion of gaseous acetylene to internal alkenes
via
1,2-difunctionalization in a desired manner is not as easy as it might be expected due to the potential competition reactions between acetylene and alkene produced and the difficulty in handling this harmful reagent and controlling the regio- and stereoselectivity. In this work, we designed an efficient catalytic system for the incorporation of acetylene gas into tremendous (
E
)-
β
-bromo vinylsulfones, which are bench-stable, easy to operate, and can function as bifunctional acetylene and show a rich reactivity profile in Sonogashira coupling, Heck coupling, substituted reaction, and various desulfonylation transformations, providing numerous internal alkenes.</description><subject>Acetylene</subject><subject>Alkenes</subject><subject>Carbon</subject><subject>Chemical engineering</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Coupling</subject><subject>Laboratories</subject><subject>Reagents</subject><subject>Stereoselectivity</subject><issn>1674-7291</issn><issn>1869-1870</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1UE1LxDAUDKLgsu4P8BbwajQfTZMcdfELFrzsPWTTZOnSbWuSKvXXm1pBL77LmzfMDI8B4JLgG4KxuI2EFLREmDJEpCBoPAELIks1Xfg041IUSFBFzsEqxgPOwximgi9AdV_7obWp7lrTwPTRIWvCrmthcGbv2gSPpnLQh-4IjXVpbFzr4HttILmmqPrjrT_NBKBpK1inCE3fN7X95uIFOPOmiW71s5dg-_iwXT-jzevTy_pugywjZUJGOFkaISvMheLWUaGwwL7YCVc4xbhXhVXMc8kzISkW1LOSek6FlRVhbAmu5tg-dG-Di0kfuiHk36KmigkisWIqq8issqGLMTiv-1AfTRg1wXqqU8916lynnurUY_bQ2ROztt278Jv8v-kLTCZ4PA</recordid><startdate>20240301</startdate><enddate>20240301</enddate><creator>Yang, Bo</creator><creator>Li, Kangkui</creator><creator>Wang, Yongdong</creator><creator>Zhu, Shifa</creator><general>Science China Press</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20240301</creationdate><title>Bifunctional two-carbon reagent made from acetylene via 1,2-difunctionalization and its applications</title><author>Yang, Bo ; Li, Kangkui ; Wang, Yongdong ; Zhu, Shifa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-a7e86a78d05795ce279070f4b7e4e935f94c93f5857e482072f362f527c8d133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acetylene</topic><topic>Alkenes</topic><topic>Carbon</topic><topic>Chemical engineering</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Coupling</topic><topic>Laboratories</topic><topic>Reagents</topic><topic>Stereoselectivity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Bo</creatorcontrib><creatorcontrib>Li, Kangkui</creatorcontrib><creatorcontrib>Wang, Yongdong</creatorcontrib><creatorcontrib>Zhu, Shifa</creatorcontrib><collection>CrossRef</collection><jtitle>Science China. Chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Bo</au><au>Li, Kangkui</au><au>Wang, Yongdong</au><au>Zhu, Shifa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bifunctional two-carbon reagent made from acetylene via 1,2-difunctionalization and its applications</atitle><jtitle>Science China. Chemistry</jtitle><stitle>Sci. China Chem</stitle><date>2024-03-01</date><risdate>2024</risdate><volume>67</volume><issue>3</issue><spage>936</spage><epage>944</epage><pages>936-944</pages><issn>1674-7291</issn><eissn>1869-1870</eissn><abstract>There are very limited approaches to directly gluing two molecules for the production of internal alkenes using the vastly abundant acetylene
via
1,2-difunctionalization. Conversion of gaseous acetylene to internal alkenes
via
1,2-difunctionalization in a desired manner is not as easy as it might be expected due to the potential competition reactions between acetylene and alkene produced and the difficulty in handling this harmful reagent and controlling the regio- and stereoselectivity. In this work, we designed an efficient catalytic system for the incorporation of acetylene gas into tremendous (
E
)-
β
-bromo vinylsulfones, which are bench-stable, easy to operate, and can function as bifunctional acetylene and show a rich reactivity profile in Sonogashira coupling, Heck coupling, substituted reaction, and various desulfonylation transformations, providing numerous internal alkenes.</abstract><cop>Beijing</cop><pub>Science China Press</pub><doi>10.1007/s11426-023-1871-y</doi><tpages>9</tpages></addata></record> |
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subjects | Acetylene Alkenes Carbon Chemical engineering Chemistry Chemistry and Materials Science Chemistry/Food Science Coupling Laboratories Reagents Stereoselectivity |
title | Bifunctional two-carbon reagent made from acetylene via 1,2-difunctionalization and its applications |
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