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dc.contributor.author강수성*
dc.date.accessioned2018-11-21T16:30:21Z-
dc.date.available2018-11-21T16:30:21Z-
dc.date.issued2018*
dc.identifier.issn0040-4039*
dc.identifier.otherOAK-23008*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/246717-
dc.description.abstractA facile method for the direct synthesis of amides from aldehydes is described. Amide bonds were synthesized by an oxidative amidation in the presence of dibromoisocyanuric acid (DBI). Treatment of aromatic and aliphatic aldehydes with dibromoisocyanuric acid generated acyl bromide intermediates, which were employed to react with a variety of secondary and primary amines to give amides. Through this reaction method, various amides were synthesized directly from aldehydes under mild conditions in high yields and short times. This facile and efficient procedure provides potential strategy for the direct synthesis of amides from aldehydes. (C) 2018 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD*
dc.subjectAmidation*
dc.subjectAldehydes*
dc.subjectDibromoisocyanuric acid*
dc.subjectAcyl bromide*
dc.titleConvenient metal-free direct oxidative amidation of aldehyde using dibromoisocyanuric acid under mild conditions*
dc.typeArticle*
dc.relation.issue39*
dc.relation.volume59*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage3541*
dc.relation.lastpage3546*
dc.relation.journaltitleTETRAHEDRON LETTERS*
dc.identifier.doi10.1016/j.tetlet.2018.08.026*
dc.identifier.wosidWOS:000450698200009*
dc.identifier.scopusid2-s2.0-85052096637*
dc.author.googleKang, Soosung*
dc.author.googleMinh Thanh La*
dc.author.googleKim, Hee-Kwon*
dc.contributor.scopusid강수성(56177300500)*
dc.date.modifydate20240527115543*
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약학대학 > 약학과 > Journal papers
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