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dc.contributor.authorChen, Kai-Chien_US
dc.contributor.authorBarve, Indrajeet J.en_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2020-03-02T03:23:28Z-
dc.date.available2020-03-02T03:23:28Z-
dc.date.issued2020-01-17en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.orglett.9b04162en_US
dc.identifier.urihttp://hdl.handle.net/11536/153741-
dc.description.abstractA catalyst-controlled highly chemoselective and regioselective intramolecular cycloamidation of triazol-1-ylbenzamides toward the synthesis of scarcely known heterocycles is reported. In the presence of a palladium catalyst, this cycloisomerization reaction afforded substituted benzotriazlolodiazepin-7-ones via intramolecular insertion of a palladium into C-C triple bond in a 7-exo-dig way. Alternatively, the use of a silver catalyst in the reaction produced substituted benzotriazolodiazocin-8-ones in a highly regioselective manner through 8-endo-dig intramolecular ring closure.en_US
dc.language.isoen_USen_US
dc.titleCatalyst-Controlled Regioselective Synthesis of Benzotriazlolodiazepin-7-ones and Benzotriazolodiazocin-8-onesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.orglett.9b04162en_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume22en_US
dc.citation.issue2en_US
dc.citation.spage428en_US
dc.citation.epage432en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000508468200018en_US
dc.citation.woscount0en_US
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