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분자활성촉매반응연구단
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Cu(I)-Catalyzed Enantioselective [5+1] Cycloaddition of N-Aromatic Compounds and Alkynes via Chelating-Assisted 1,2-Dearomative Addition

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dc.contributor.authorNirupam De-
dc.contributor.authorDonguk Ko-
dc.contributor.authorSeung-yeol Baek-
dc.contributor.authorChangjin Oh-
dc.contributor.authorJiyoung Kim-
dc.contributor.authorMu-Hyun Baik-
dc.contributor.authorEun Jeong Yoo-
dc.date.accessioned2020-12-22T02:31:50Z-
dc.date.accessioned2020-12-22T02:31:50Z-
dc.date.available2020-12-22T02:31:50Z-
dc.date.available2020-12-22T02:31:50Z-
dc.date.created2020-11-16-
dc.date.issued2020-10-
dc.identifier.issn2155-5435-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/7589-
dc.description.abstract© 2020 American Chemical Society. Copper-catalyzed [5 + 1] cycloadditions of N-aromatic zwitterions have been accomplished by chelation-assisted 1,2-dearomative addition of electron-deficient terminal alkynes. The unique modular skeleton of pyrazino[1,2-a]quinoline could be obtained from the regio- and stereoselective cascade annulation process, which was supported by computational studies. Further, an asymmetric variant of the developed strategy has been successfully extended for enabling access to optically enriched six-member cyclic systems-
dc.description.uri1-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.titleCu(I)-Catalyzed Enantioselective [5+1] Cycloaddition of N-Aromatic Compounds and Alkynes via Chelating-Assisted 1,2-Dearomative Addition-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000577156300008-
dc.identifier.scopusid2-s2.0-85096209807-
dc.identifier.rimsid73498-
dc.contributor.affiliatedAuthorSeung-yeol Baek-
dc.contributor.affiliatedAuthorChangjin Oh-
dc.contributor.affiliatedAuthorMu-Hyun Baik-
dc.identifier.doi10.1021/acscatal.0c03014-
dc.identifier.bibliographicCitationACS CATALYSIS, v.10, no.19, pp.10905 - 10913-
dc.citation.titleACS CATALYSIS-
dc.citation.volume10-
dc.citation.number19-
dc.citation.startPage10905-
dc.citation.endPage10913-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusREISSERT-TYPE REACTION-
dc.subject.keywordPlusDIELS-ALDER REACTIONS-
dc.subject.keywordPlusDIVERGENT SYNTHESIS-
dc.subject.keywordPlusAZOMETHINE IMINES-
dc.subject.keywordPlusVINYLCYCLOPROPANES-
dc.subject.keywordPlusTRIMETHYLENEMETHANE-
dc.subject.keywordPlusREACTIVITY-
dc.subject.keywordPlusQUINOLINES-
dc.subject.keywordPlus1,4-ENYNE-
dc.subject.keywordPlusSALTS-
dc.subject.keywordAuthorheterocycles-
dc.subject.keywordAuthorcycloaddition-
dc.subject.keywordAuthordearomatization-
dc.subject.keywordAuthorsite selectivity-
dc.subject.keywordAuthorstereoselectivity-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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