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| ファイル | 記述 | サイズ | フォーマット | |
|---|---|---|---|---|
| acs.orglett.0c03782.pdf | 691.97 kB | Adobe PDF | 見る/開く |
完全メタデータレコード
| DCフィールド | 値 | 言語 |
|---|---|---|
| dc.contributor.author | Yamada, Kodai | en |
| dc.contributor.author | Yanagi, Tomoyuki | en |
| dc.contributor.author | Yorimitsu, Hideki | en |
| dc.contributor.alternative | 山田, 航大 | ja |
| dc.contributor.alternative | 柳, 智征 | ja |
| dc.contributor.alternative | 依光, 英樹 | ja |
| dc.date.accessioned | 2021-01-15T06:13:42Z | - |
| dc.date.available | 2021-01-15T06:13:42Z | - |
| dc.date.issued | 2020-12-18 | - |
| dc.identifier.issn | 1523-7060 | - |
| dc.identifier.issn | 1523-7052 | - |
| dc.identifier.uri | http://hdl.handle.net/2433/261022 | - |
| dc.description.abstract | Readily available aryldimethylsulfonium triflates react with zinc powder under nickel catalysis via the selective cleavage of the sp2-hybridized carbon–sulfur bond to produce salt-free arylzinc triflates under mild conditions. This zincation displays superb chemoselectivity and thus represents a protocol that is complementary or orthogonal to existing methods. The generated arylzinc reagents show both high reactivity and chemoselectivity in palladium-catalyzed and copper-mediated cross-coupling reactions. | en |
| dc.format.mimetype | application/pdf | - |
| dc.language.iso | eng | - |
| dc.publisher | American Chemical Society | en |
| dc.rights | This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.0c03782. | en |
| dc.rights | The full-text file will be made open to the public on 10 December 2021 in accordance with publisher's 'Terms and Conditions for Self-Archiving'. | en |
| dc.rights | This is not the published version. Please cite only the published version. | en |
| dc.rights | この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。 | ja |
| dc.title | Generation of Organozinc Reagents from Arylsulfonium Salts Using a Nickel Catalyst and Zinc Dust | en |
| dc.type | journal article | - |
| dc.type.niitype | Journal Article | - |
| dc.identifier.jtitle | Organic Letters | en |
| dc.identifier.volume | 22 | - |
| dc.identifier.issue | 24 | - |
| dc.identifier.spage | 9712 | - |
| dc.identifier.epage | 9718 | - |
| dc.relation.doi | 10.1021/acs.orglett.0c03782 | - |
| dc.textversion | author | - |
| dc.address | Department of Chemistry, Graduate School of Science, Kyoto University | en |
| dc.address | Department of Chemistry, Graduate School of Science, Kyoto University | en |
| dc.address | Department of Chemistry, Graduate School of Science, Kyoto University | en |
| dc.identifier.pmid | 33300805 | - |
| dcterms.accessRights | open access | - |
| datacite.date.available | 2021-11-10 | - |
| datacite.awardNumber | JP19H00895 | - |
| jpcoar.funderName | 日本学術振興会 | ja |
| jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
| 出現コレクション: | 学術雑誌掲載論文等 | |
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