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alpha-Hydroxy acid as an aldehyde surrogate: metal-free synthesis of pyrrolo[1,2-a]quinoxalines, quinazolinones, and other N-heterocyclesviadecarboxylative oxidative annulation reaction

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dc.contributor.authorViji, Mayavan-
dc.contributor.authorVishwanath, Manjunatha-
dc.contributor.authorSim, Jaeuk-
dc.contributor.authorPark, Yunjeong-
dc.contributor.authorJung, Chanhyun-
dc.contributor.authorLee, Seohu-
dc.contributor.authorLee, Heesoon-
dc.contributor.authorLee, Kiho-
dc.contributor.authorJung, Jae-Kyung-
dc.date.accessioned2021-08-30T10:54:15Z-
dc.date.available2021-08-30T10:54:15Z-
dc.date.created2021-06-19-
dc.date.issued2020-10-11-
dc.identifier.issn2046-2069-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/52467-
dc.description.abstractA metal-free and efficient procedure for the synthesis of pyrrolo[1,2-a]quinoxalines, quinazolinones, and indolo[1,2-a]quinoxaline has been developed. The key features of our method include thein situgeneration of aldehyde from alpha-hydroxy acid in the presence of TBHP (tert-butyl hydrogen peroxide), and further condensation with various amines, followed by intramolecular cyclization and subsequent oxidation to afford the corresponding quinoxalines, quinazolinones derivatives in moderate to high yields.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectONE-POT SYNTHESIS-
dc.subjectCOPPER-CATALYZED SYNTHESIS-
dc.subject2,3-DISUBSTITUTED QUINAZOLIN-4(3H)-ONES-
dc.subjectANTIMALARIAL ACTIVITY-
dc.subjectPOTENTIAL INHIBITORS-
dc.subjectEFFICIENT SYNTHESIS-
dc.subjectPHENYLACETIC ACIDS-
dc.subjectBOND ACTIVATION-
dc.subjectDERIVATIVES-
dc.subjectCYCLIZATION-
dc.titlealpha-Hydroxy acid as an aldehyde surrogate: metal-free synthesis of pyrrolo[1,2-a]quinoxalines, quinazolinones, and other N-heterocyclesviadecarboxylative oxidative annulation reaction-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Kiho-
dc.identifier.doi10.1039/d0ra07093a-
dc.identifier.scopusid2-s2.0-85093821555-
dc.identifier.wosid000578727600029-
dc.identifier.bibliographicCitationRSC ADVANCES, v.10, no.61, pp.37202 - 37208-
dc.relation.isPartOfRSC ADVANCES-
dc.citation.titleRSC ADVANCES-
dc.citation.volume10-
dc.citation.number61-
dc.citation.startPage37202-
dc.citation.endPage37208-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusONE-POT SYNTHESIS-
dc.subject.keywordPlusCOPPER-CATALYZED SYNTHESIS-
dc.subject.keywordPlus2,3-DISUBSTITUTED QUINAZOLIN-4(3H)-ONES-
dc.subject.keywordPlusANTIMALARIAL ACTIVITY-
dc.subject.keywordPlusPOTENTIAL INHIBITORS-
dc.subject.keywordPlusEFFICIENT SYNTHESIS-
dc.subject.keywordPlusPHENYLACETIC ACIDS-
dc.subject.keywordPlusBOND ACTIVATION-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusCYCLIZATION-
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