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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
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Oh, Sang-Ha | - |
| dc.contributor.author | Oh, Joo-Yeon | - |
| dc.contributor.author | Vo, Ngoc Binh | - |
| dc.contributor.author | Ngo, Quoc Anh | - |
| dc.contributor.author | Kovalenko, Vitaly | - |
| dc.contributor.author | Cho, Cheon-Gyu | - |
| dc.date.accessioned | 2026-04-03T02:30:18Z | - |
| dc.date.available | 2026-04-03T02:30:18Z | - |
| dc.date.issued | 2024-09 | - |
| dc.identifier.issn | 0022-3263 | - |
| dc.identifier.issn | 1520-6904 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/211945 | - |
| dc.description.abstract | A 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.extent | 10 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | American Chemical Society | - |
| dc.title | 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 | - |
| dc.title.alternative | 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 | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1021/acs.joc.4c01696 | - |
| dc.identifier.scopusid | 2-s2.0-85202979290 | - |
| dc.identifier.wosid | 001302834400001 | - |
| dc.identifier.bibliographicCitation | The Journal of Organic Chemistry, v.89, no.18, pp 13501 - 13510 | - |
| dc.citation.title | The Journal of Organic Chemistry | - |
| dc.citation.volume | 89 | - |
| dc.citation.number | 18 | - |
| dc.citation.startPage | 13501 | - |
| dc.citation.endPage | 13510 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.subject.keywordPlus | ALKALOIDS | - |
| dc.subject.keywordPlus | CHEMISTRY | - |
| dc.subject.keywordPlus | INDOLINES | - |
| dc.subject.keywordPlus | NITRILES | - |
| dc.subject.keywordPlus | STRATEGY | - |
| dc.identifier.url | https://pubs.acs.org/doi/10.1021/acs.joc.4c01696 | - |
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