完整後設資料紀錄
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dc.contributor.authorUeda, Mitsuhiroen_US
dc.contributor.authorUeno, Tamamien_US
dc.contributor.authorSuyama, Yukien_US
dc.contributor.authorRyu, Ilhyongen_US
dc.date.accessioned2018-08-21T05:54:19Z-
dc.date.available2018-08-21T05:54:19Z-
dc.date.issued2017-07-26en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tetlet.2017.06.049en_US
dc.identifier.urihttp://hdl.handle.net/11536/145809-
dc.description.abstractTreatment of alkynes with ortho-formyl and acetyl phenylboronic acids in the presence of a cobalt catalyst resulted in the formation of 2,3-disubstituted indenols in good yields. When aryl silyl alkynes were used, 2-aryl-3-silyl indenols were obtained regioselectively in good yields. (C) 2017 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subject2,3-Disubstituted indenolen_US
dc.subjectSilyl aryl alkyneen_US
dc.subjectCobalten_US
dc.subject[3+2] annulationen_US
dc.subjectortho-Carbonylated phenylboronic aciden_US
dc.titleCobalt-catalyzed regioselective [3+2] annulation of ortho-formyl and acetyl substituted phenylboronic acids with alkynesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tetlet.2017.06.049en_US
dc.identifier.journalTETRAHEDRON LETTERSen_US
dc.citation.volume58en_US
dc.citation.spage2972en_US
dc.citation.epage2974en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000405973600024en_US
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