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Asymmetric Formal Total Syntheses of (+)- and (-)-Limaspermidine from Chirally Resolved 2-Pyrone Diels-Alder Cycloadducts via Aromatic C-H Amidation and Imino-Diels-Alder Reaction

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dc.contributor.authorOh, Sang-Ha-
dc.contributor.authorOh, Joo-Yeon-
dc.contributor.authorVo, Ngoc Binh-
dc.contributor.authorNgo, Quoc Anh-
dc.contributor.authorKovalenko, Vitaly-
dc.contributor.authorCho, Cheon-Gyu-
dc.date.accessioned2026-04-03T02:30:18Z-
dc.date.available2026-04-03T02:30:18Z-
dc.date.issued2024-09-
dc.identifier.issn0022-3263-
dc.identifier.issn1520-6904-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/211945-
dc.description.abstractA new asymmetric synthetic route to (+)- and (−)-limaspermidine was devised, starting with chirally resolved enantiomerically pure 2-pyrone Diels–Alder cycloadducts. This route utilizes intramolecular Pd-catalyzed aromatic C–H amidation and imino-Diels–Alder reactions to construct the key indoline and indolizidine subunits onto the central cyclohexane core, allowing the straightforward formal total syntheses of both (+)- and (−)-limaspermidine.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleAsymmetric Formal Total Syntheses of (+)- and (-)-Limaspermidine from Chirally Resolved 2-Pyrone Diels-Alder Cycloadducts via Aromatic C-H Amidation and Imino-Diels-Alder Reaction-
dc.title.alternativeAsymmetric Formal Total Syntheses of (+)- and (−)-Limaspermidine from Chirally Resolved 2-Pyrone Diels-Alder Cycloadducts via Aromatic C-H Amidation and Imino-Diels-Alder Reaction-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acs.joc.4c01696-
dc.identifier.scopusid2-s2.0-85202979290-
dc.identifier.wosid001302834400001-
dc.identifier.bibliographicCitationThe Journal of Organic Chemistry, v.89, no.18, pp 13501 - 13510-
dc.citation.titleThe Journal of Organic Chemistry-
dc.citation.volume89-
dc.citation.number18-
dc.citation.startPage13501-
dc.citation.endPage13510-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusINDOLINES-
dc.subject.keywordPlusNITRILES-
dc.subject.keywordPlusSTRATEGY-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acs.joc.4c01696-
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