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dc.contributor.authorKaga, Atsushien
dc.contributor.authorIida, Hirokazuen
dc.contributor.authorTsuchiya, Shunen
dc.contributor.authorSaito, Hayateen
dc.contributor.authorNakano, Kojien
dc.contributor.authorYorimitsu, Hidekien
dc.contributor.alternative加賀, 敦志ja
dc.contributor.alternative土屋, 駿ja
dc.contributor.alternative齊藤, 颯ja
dc.contributor.alternative依光, 英樹ja
dc.date.accessioned2022-03-10T09:06:57Z-
dc.date.available2022-03-10T09:06:57Z-
dc.date.issued2021-03-
dc.identifier.urihttp://hdl.handle.net/2433/268764-
dc.description.abstractA new mode of aromatic metamorphosis has been developed, which allows thiophenes and their benzo-fused derivatives to be converted to a variety of exotic heteroles. This transformation involves 1) the efficient generation of key 1, 4-dianions by means of desulfurative dilithiation with lithium powder and 2) the subsequent trapping of the dianions with heteroatom electrophiles in a one-pot manner. Via the desulfurative dilithiation, the sulfur atoms of thiophenes are replaced also with a carbon–carbon double bond or a 1, 2-phenylene for the construction of benzene rings.en
dc.language.isoeng-
dc.publisherWileyen
dc.rightsThis is the peer reviewed version of the following article: [A. Kaga, H. Iida, S. Tsuchiya, H. Saito, K. Nakano, H. Yorimitsu, Chem. Eur. J. 2021, 27, 4567.], which has been published in final form at https://doi.org/10.1002/chem.202005223. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.en
dc.rightsThe full-text file will be made open to the public on 05 February 2022 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.en
dc.rightsThis is not the published version. Please cite only the published version. 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。en
dc.subjectdesulfurizationen
dc.subjectdianionen
dc.subjectheteroleen
dc.subjectlithium metalen
dc.subjectthiopheneen
dc.titleAromatic Metamorphosis of Thiophenes by Means of Desulfurative Dilithiationen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleChemistry – A European Journalen
dc.identifier.volume27-
dc.identifier.issue14-
dc.identifier.spage4567-
dc.identifier.epage4572-
dc.relation.doi10.1002/chem.202005223-
dc.textversionauthor-
dc.identifier.pmid33349986-
dcterms.accessRightsopen access-
datacite.date.available2022-02-05-
datacite.awardNumber18H04254-
datacite.awardNumber18H04409-
datacite.awardNumber19H00895-
datacite.awardNumber18J22838-
datacite.awardNumber20J01639-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PUBLICLY-18H04254/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PUBLICLY-18H04409/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19H00895/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18J22838/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-20J01639/-
dc.identifier.pissn0947-6539-
dc.identifier.eissn1521-3765-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitleアート錯体の精密制御によるヘテロ芳香環の開環と原子挿入ja
jpcoar.awardTitleフロー系が可能にするプメラー型ビアリール構築による中分子合成ja
jpcoar.awardTitle芳香環の還元的破壊に基づく有機合成ja
jpcoar.awardTitle遷移金属触媒を用いたボラサイクルの新規合成法の開発ja
jpcoar.awardTitle金属リチウムの強還元能を鍵としたヘテロπ共役系骨格の構築ja
出現コレクション:学術雑誌掲載論文等

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