DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Hyunwoo | ko |
dc.contributor.author | Park, Gyeongtae | ko |
dc.contributor.author | Park, Juhyeon | ko |
dc.contributor.author | Chang, Sukbok | ko |
dc.date.accessioned | 2016-10-07T09:26:44Z | - |
dc.date.available | 2016-10-07T09:26:44Z | - |
dc.date.created | 2016-10-05 | - |
dc.date.created | 2016-10-05 | - |
dc.date.issued | 2016-09 | - |
dc.identifier.citation | ACS CATALYSIS, v.6, no.9, pp.5922 - 5929 | - |
dc.identifier.issn | 2155-5435 | - |
dc.identifier.uri | http://hdl.handle.net/10203/213212 | - |
dc.description.abstract | Described herein is the development of Ir(III)-catalyzed direct C-H amidation using azidoformates as a readily deprotectable amino source. Substrates with unactivated methyl C(sp(3))-H and aromatic or olefinic C(sp(2)) -H bonds were smoothly reacted by the iridium-based catalyst system to provide the corresponding primary alkylamines and anilines upon the subsequent removal of N-protecting groups, such as Boc, Fmoc, Cbz, pNZ, or Troc. A brief mechanistic study and synthetic applications are also presented | - |
dc.language | English | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | IRON(II)-MEDIATED NITRENE TRANSFER | - |
dc.subject | TRANSITION-METAL-COMPLEXES | - |
dc.subject | CATALYZED DIRECT AMINATION | - |
dc.subject | BOND-FORMING REACTIONS | - |
dc.subject | ROOM-TEMPERATURE | - |
dc.subject | NITROGEN-SOURCE | - |
dc.subject | ARYL HALIDES | - |
dc.subject | INTERMOLECULAR AMIDATION | - |
dc.subject | 2,2,2-TRICHLOROETHOXYCARBONYL AZIDE | - |
dc.subject | ASYMMETRIC CATALYSIS | - |
dc.title | A Facile Access to Primary Alkylamines and Anilines via Ir(III)-Catalyzed C-H Amidation Using Azidoformates | - |
dc.type | Article | - |
dc.identifier.wosid | 000382714000031 | - |
dc.identifier.scopusid | 2-s2.0-84984863513 | - |
dc.type.rims | ART | - |
dc.citation.volume | 6 | - |
dc.citation.issue | 9 | - |
dc.citation.beginningpage | 5922 | - |
dc.citation.endingpage | 5929 | - |
dc.citation.publicationname | ACS CATALYSIS | - |
dc.identifier.doi | 10.1021/acscatal.6b01869 | - |
dc.contributor.localauthor | Chang, Sukbok | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordAuthor | C-H amidation | - |
dc.subject.keywordAuthor | iridium catalysis | - |
dc.subject.keywordAuthor | azidoformates | - |
dc.subject.keywordAuthor | primary alkylamines | - |
dc.subject.keywordAuthor | primary anilines | - |
dc.subject.keywordPlus | IRON(II)-MEDIATED NITRENE TRANSFER | - |
dc.subject.keywordPlus | TRANSITION-METAL-COMPLEXES | - |
dc.subject.keywordPlus | CATALYZED DIRECT AMINATION | - |
dc.subject.keywordPlus | BOND-FORMING REACTIONS | - |
dc.subject.keywordPlus | ROOM-TEMPERATURE | - |
dc.subject.keywordPlus | NITROGEN-SOURCE | - |
dc.subject.keywordPlus | ARYL HALIDES | - |
dc.subject.keywordPlus | INTERMOLECULAR AMIDATION | - |
dc.subject.keywordPlus | 2,2,2-TRICHLOROETHOXYCARBONYL AZIDE | - |
dc.subject.keywordPlus | ASYMMETRIC CATALYSIS | - |
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