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Dehydrogenative Amide Synthesis: Azide as a Nitrogen Source

DC Field Value Language
dc.contributor.authorZengqian Fu-
dc.contributor.authorJeongbin Lee-
dc.contributor.authorByungjoon Kang-
dc.contributor.authorSoon Hyeok Hong-
dc.date.available2015-04-20T06:32:49Z-
dc.date.created2014-08-11-
dc.date.issued2012-12-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/1205-
dc.description.abstractA new atom-economical strategy to amide linkage from an azide and alcohol liberating hydrogen and nitrogen was developed with an in situ generated ruthenium catalytic system. The reaction has broad substrate generality including diols for the synthesis of cyclic imides.-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.titleDehydrogenative Amide Synthesis: Azide as a Nitrogen Source-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000311926000055-
dc.identifier.scopusid2-s2.0-84870908624-
dc.identifier.rimsid287ko
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorJeongbin Lee-
dc.contributor.affiliatedAuthorByungjoon Kang-
dc.contributor.affiliatedAuthorSoon Hyeok Hong-
dc.identifier.doi10.1021/ol302915g-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.14, no.23, pp.6028 - 6031-
dc.relation.isPartOfORGANIC LETTERS-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume14-
dc.citation.number23-
dc.citation.startPage6028-
dc.citation.endPage6031-
dc.date.scptcdate2018-10-01-
dc.description.wostc37-
dc.description.scptc39-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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Center for Nanoparticle Research(나노입자 연구단) > 1. Journal Papers (저널논문)
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