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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Science China. Chemistry 2024-03, Vol.67 (3), p.936-944
Hauptverfasser: Yang, Bo, Li, Kangkui, Wang, Yongdong, Zhu, Shifa
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 944
container_issue 3
container_start_page 936
container_title Science China. Chemistry
container_volume 67
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
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2937180939</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2937180939</sourcerecordid><originalsourceid>FETCH-LOGICAL-c316t-a7e86a78d05795ce279070f4b7e4e935f94c93f5857e482072f362f527c8d133</originalsourceid><addsrcrecordid>eNp1UE1LxDAUDKLgsu4P8BbwajQfTZMcdfELFrzsPWTTZOnSbWuSKvXXm1pBL77LmzfMDI8B4JLgG4KxuI2EFLREmDJEpCBoPAELIks1Xfg041IUSFBFzsEqxgPOwximgi9AdV_7obWp7lrTwPTRIWvCrmthcGbv2gSPpnLQh-4IjXVpbFzr4HttILmmqPrjrT_NBKBpK1inCE3fN7X95uIFOPOmiW71s5dg-_iwXT-jzevTy_pugywjZUJGOFkaISvMheLWUaGwwL7YCVc4xbhXhVXMc8kzISkW1LOSek6FlRVhbAmu5tg-dG-Di0kfuiHk36KmigkisWIqq8issqGLMTiv-1AfTRg1wXqqU8916lynnurUY_bQ2ROztt278Jv8v-kLTCZ4PA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2937180939</pqid></control><display><type>article</type><title>Bifunctional two-carbon reagent made from acetylene via 1,2-difunctionalization and its applications</title><source>Alma/SFX Local Collection</source><source>SpringerLink Journals - AutoHoldings</source><creator>Yang, Bo ; Li, Kangkui ; Wang, Yongdong ; Zhu, Shifa</creator><creatorcontrib>Yang, Bo ; Li, Kangkui ; Wang, Yongdong ; Zhu, Shifa</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 1674-7291
ispartof Science China. Chemistry, 2024-03, Vol.67 (3), p.936-944
issn 1674-7291
1869-1870
language eng
recordid cdi_proquest_journals_2937180939
source Alma/SFX Local Collection; SpringerLink Journals - AutoHoldings
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T14%3A25%3A26IST&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=Bifunctional%20two-carbon%20reagent%20made%20from%20acetylene%20via%201,2-difunctionalization%20and%20its%20applications&rft.jtitle=Science%20China.%20Chemistry&rft.au=Yang,%20Bo&rft.date=2024-03-01&rft.volume=67&rft.issue=3&rft.spage=936&rft.epage=944&rft.pages=936-944&rft.issn=1674-7291&rft.eissn=1869-1870&rft_id=info:doi/10.1007/s11426-023-1871-y&rft_dat=%3Cproquest_cross%3E2937180939%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=2937180939&rft_id=info:pmid/&rfr_iscdi=true