Catalytic Dearomatization of N-Heteroarenes with Silicon and Boron Compounds

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dc.contributor.authorPark, Sehoonko
dc.contributor.authorChang, Sukbokko
dc.date.accessioned2017-07-18T06:31:01Z-
dc.date.available2017-07-18T06:31:01Z-
dc.date.created2017-07-10-
dc.date.created2017-07-10-
dc.date.issued2017-06-
dc.identifier.citationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.56, no.27, pp.7720 - 7738-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10203/224871-
dc.description.abstractDearomatized N-heterocycles are an important class of structural motifs for organic synthesis and chemical biology. The catalytic dearomative reduction of unactivated N-heteroarenes using silicon and/ or boron-containing compounds as a reductant is one of the most straightforward alternatives to hydrogenation. However, thus far, there are few reported examples on the catalytic reduction of N-heteroaromatic compounds with silane or borane reducing agents. This Review presents recent advances in the catalytic reduction of unactivated N-heteroarenes by hydrosilanes, hydroboranes, silaboranes, and diboranes. The focus is on the chemical reactivity and selectivity of transition-metal or metal-free organocatalyst systems. In addition, the working modes of these catalysis will be described primarily on the basis of experimental mechanistic insight.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectTRANSITION-METAL-COMPLEXES-
dc.subjectTRANSFER HYDROGENATION-
dc.subjectPARTIAL REDUCTION-
dc.subjectREGIOSELECTIVE 1,4-HYDROBORATION-
dc.subjectASYMMETRIC HYDROGENATION-
dc.subjectSILYLATIVE REDUCTION-
dc.subjectCARBONYL-COMPOUNDS-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectINDOLE ALKALOIDS-
dc.subjectHANTZSCH ESTERS-
dc.titleCatalytic Dearomatization of N-Heteroarenes with Silicon and Boron Compounds-
dc.typeArticle-
dc.identifier.wosid000403839000004-
dc.identifier.scopusid2-s2.0-85020169770-
dc.type.rimsART-
dc.citation.volume56-
dc.citation.issue27-
dc.citation.beginningpage7720-
dc.citation.endingpage7738-
dc.citation.publicationnameANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.identifier.doi10.1002/anie.201612140-
dc.contributor.localauthorChang, Sukbok-
dc.contributor.nonIdAuthorPark, Sehoon-
dc.description.isOpenAccessN-
dc.type.journalArticleReview-
dc.subject.keywordAuthorboration-
dc.subject.keywordAuthorcatalytic reduction-
dc.subject.keywordAuthordearomatization-
dc.subject.keywordAuthorN-heteroarenes-
dc.subject.keywordAuthorsilylation-
dc.subject.keywordPlusTRANSITION-METAL-COMPLEXES-
dc.subject.keywordPlusTRANSFER HYDROGENATION-
dc.subject.keywordPlusPARTIAL REDUCTION-
dc.subject.keywordPlusREGIOSELECTIVE 1,4-HYDROBORATION-
dc.subject.keywordPlusASYMMETRIC HYDROGENATION-
dc.subject.keywordPlusSILYLATIVE REDUCTION-
dc.subject.keywordPlusCARBONYL-COMPOUNDS-
dc.subject.keywordPlusORGANIC-SYNTHESIS-
dc.subject.keywordPlusINDOLE ALKALOIDS-
dc.subject.keywordPlusHANTZSCH ESTERS-
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