Preparation of (E)‑1,3-Enyne Derivatives through Palladium Catalyzed Hydroalkynylation of Allenes
A general and efficient palladium catalyzed hydroalkynylation of allenes was developed to produce synthetically versatile (E)-1,3-enyne derivatives with high regio- and stereoselectivity. This catalytic system proceeded under mild conditions and was compatible with a broad range of substrates, espec...
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Veröffentlicht in: | Journal of organic chemistry 2022-01, Vol.87 (2), p.1589-1597 |
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container_title | Journal of organic chemistry |
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creator | Liu, Zhi-Kai Yang, Ying Zhan, Zhuang-Ping |
description | A general and efficient palladium catalyzed hydroalkynylation of allenes was developed to produce synthetically versatile (E)-1,3-enyne derivatives with high regio- and stereoselectivity. This catalytic system proceeded under mild conditions and was compatible with a broad range of substrates, especially for allenes without electron-bias groups. This work further broadens the synthetic potential of these scaffolds in organic synthesis and medicinal chemistry. |
doi_str_mv | 10.1021/acs.joc.1c02732 |
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This work further broadens the synthetic potential of these scaffolds in organic synthesis and medicinal chemistry.</description><identifier>ISSN: 0022-3263</identifier><identifier>EISSN: 1520-6904</identifier><identifier>DOI: 10.1021/acs.joc.1c02732</identifier><identifier>PMID: 34967640</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Alkadienes ; Catalysis ; Palladium ; Stereoisomerism</subject><ispartof>Journal of organic chemistry, 2022-01, Vol.87 (2), p.1589-1597</ispartof><rights>2021 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a333t-7eae90370aea4f75272fdc05a2f4c2b8acbd345376600f2a0336eaafa0294133</citedby><cites>FETCH-LOGICAL-a333t-7eae90370aea4f75272fdc05a2f4c2b8acbd345376600f2a0336eaafa0294133</cites><orcidid>0000-0002-6310-8663</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02732$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.joc.1c02732$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,777,781,2752,27057,27905,27906,56719,56769</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34967640$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Zhi-Kai</creatorcontrib><creatorcontrib>Yang, Ying</creatorcontrib><creatorcontrib>Zhan, Zhuang-Ping</creatorcontrib><title>Preparation of (E)‑1,3-Enyne Derivatives through Palladium Catalyzed Hydroalkynylation of Allenes</title><title>Journal of organic chemistry</title><addtitle>J. Org. Chem</addtitle><description>A general and efficient palladium catalyzed hydroalkynylation of allenes was developed to produce synthetically versatile (E)-1,3-enyne derivatives with high regio- and stereoselectivity. This catalytic system proceeded under mild conditions and was compatible with a broad range of substrates, especially for allenes without electron-bias groups. 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Org. Chem</addtitle><date>2022-01-21</date><risdate>2022</risdate><volume>87</volume><issue>2</issue><spage>1589</spage><epage>1597</epage><pages>1589-1597</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><abstract>A general and efficient palladium catalyzed hydroalkynylation of allenes was developed to produce synthetically versatile (E)-1,3-enyne derivatives with high regio- and stereoselectivity. This catalytic system proceeded under mild conditions and was compatible with a broad range of substrates, especially for allenes without electron-bias groups. This work further broadens the synthetic potential of these scaffolds in organic synthesis and medicinal chemistry.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>34967640</pmid><doi>10.1021/acs.joc.1c02732</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6310-8663</orcidid></addata></record> |
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source | MEDLINE; ACS Publications |
subjects | Alkadienes Catalysis Palladium Stereoisomerism |
title | Preparation of (E)‑1,3-Enyne Derivatives through Palladium Catalyzed Hydroalkynylation of Allenes |
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