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Metal-free approach for the L-proline mediated synthesis of nitrones from nitrosobenzene

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dc.contributor.authorChoi, Minho-
dc.contributor.authorViji, Mayavan-
dc.contributor.authorKim, Donghwan-
dc.contributor.authorLee, Young Hee-
dc.contributor.authorSim, Jaeuk-
dc.contributor.authorKwak, Young-Shin-
dc.contributor.authorLee, Kiho-
dc.contributor.authorLee, Heesoon-
dc.contributor.authorJung, Jae-Kyung-
dc.date.accessioned2021-09-02T07:52:39Z-
dc.date.available2021-09-02T07:52:39Z-
dc.date.created2021-06-16-
dc.date.issued2018-08-02-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/73798-
dc.description.abstractAn efficient, and metal-free approach for the L-proline mediated synthesis of nitrones from nitro-sobenzene and benzaldehydes has been established. The reaction undergoes very efficiently at room temperature in methanol as a solvent. The reaction is assumed to involve that the initial formation of azomethine ylide and [2 + 3] cycloaddition of nitrosobenzene, followed by the subsequent retro [2 + 3] cycloaddition could offer the desired nitrone. (c) 2018 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectCOPE-TYPE HYDROAMINATION-
dc.subjectN-ARYLATION PROCESS-
dc.subjectALPHA-AMINO-ACIDS-
dc.subjectONE-POT SYNTHESIS-
dc.subjectAZOMETHINE YLIDE-
dc.subjectCYCLOADDITION REACTIONS-
dc.subjectASYMMETRIC 1,3-DIPOLAR-
dc.subjectN,N-DISUBSTITUTED HYDROXYLAMINES-
dc.subjectCATALYTIC-OXIDATION-
dc.subjectREDUCTIVE APPROACH-
dc.titleMetal-free approach for the L-proline mediated synthesis of nitrones from nitrosobenzene-
dc.typeArticle-
dc.contributor.affiliatedAuthorKwak, Young-Shin-
dc.contributor.affiliatedAuthorLee, Kiho-
dc.identifier.doi10.1016/j.tet.2018.06.001-
dc.identifier.scopusid2-s2.0-85048495957-
dc.identifier.wosid000439403400005-
dc.identifier.bibliographicCitationTETRAHEDRON, v.74, no.31, pp.4182 - 4187-
dc.relation.isPartOfTETRAHEDRON-
dc.citation.titleTETRAHEDRON-
dc.citation.volume74-
dc.citation.number31-
dc.citation.startPage4182-
dc.citation.endPage4187-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusCOPE-TYPE HYDROAMINATION-
dc.subject.keywordPlusN-ARYLATION PROCESS-
dc.subject.keywordPlusALPHA-AMINO-ACIDS-
dc.subject.keywordPlusONE-POT SYNTHESIS-
dc.subject.keywordPlusAZOMETHINE YLIDE-
dc.subject.keywordPlusCYCLOADDITION REACTIONS-
dc.subject.keywordPlusASYMMETRIC 1,3-DIPOLAR-
dc.subject.keywordPlusN,N-DISUBSTITUTED HYDROXYLAMINES-
dc.subject.keywordPlusCATALYTIC-OXIDATION-
dc.subject.keywordPlusREDUCTIVE APPROACH-
dc.subject.keywordAuthorNitrones-
dc.subject.keywordAuthorMetal-free-
dc.subject.keywordAuthorL-proline-
dc.subject.keywordAuthorNitrosobenzene-
dc.subject.keywordAuthorAzomethine ylide-
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