A Regio- and Diastereoselective Stille Coupling/Intramolecular Diels-Alder Cascade for the Generation of Fused Pyridines and Application in the Synthesis of (+)-Lycopladine A and (-)-Lycoposerramine R
DC Field | Value | Language |
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dc.contributor.author | Sim, Kyu-Hyun | - |
dc.contributor.author | ul Ansari, Thameem | - |
dc.contributor.author | Park, Yong-Gyu | - |
dc.contributor.author | Jeong, Yeolib | - |
dc.contributor.author | Oh, Sang-Ha | - |
dc.contributor.author | Min, Hye-Won | - |
dc.contributor.author | Jeon, Da-Yoon | - |
dc.contributor.author | Kim, Hyunwoo | - |
dc.contributor.author | Cho, Cheon-Gyu | - |
dc.date.accessioned | 2023-07-05T02:45:13Z | - |
dc.date.available | 2023-07-05T02:45:13Z | - |
dc.date.created | 2022-10-06 | - |
dc.date.issued | 2022-09 | - |
dc.identifier.issn | 1433-7851 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/186137 | - |
dc.description.abstract | 2-Pyrones with a chiral branched allylic silyl ether substituent underwent intramolecular Diels-Alder reactions with remarkably high pi-facial- and endo-selectivities. The resulting diastereomerically and enantiomerically pure cycloadducts were transformed into the natural products (+)-lycopladine A and (-)-lycoposerramine R. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | WILEY-V C H VERLAG GMBH | - |
dc.title | A Regio- and Diastereoselective Stille Coupling/Intramolecular Diels-Alder Cascade for the Generation of Fused Pyridines and Application in the Synthesis of (+)-Lycopladine A and (-)-Lycoposerramine R | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Cho, Cheon-Gyu | - |
dc.identifier.doi | 10.1002/anie.202212016 | - |
dc.identifier.scopusid | 2-s2.0-85138812531 | - |
dc.identifier.wosid | 000857817600001 | - |
dc.identifier.bibliographicCitation | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.61, no.42, pp.1 - 5 | - |
dc.relation.isPartOf | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | - |
dc.citation.title | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | - |
dc.citation.volume | 61 | - |
dc.citation.number | 42 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 5 | - |
dc.type.rims | ART | - |
dc.type.docType | Article; Early Access | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.subject.keywordPlus | HIGHLY SUBSTITUTED PYRIDINES | - |
dc.subject.keywordPlus | 2+2+2 CYCLOADDITION | - |
dc.subject.keywordPlus | ALLYLIC ETHERIFICATION | - |
dc.subject.keywordPlus | 3,5-DIBROMO-2-PYRONE | - |
dc.subject.keywordPlus | CONSTRUCTION | - |
dc.subject.keywordPlus | CYCLIZATIONS | - |
dc.subject.keywordPlus | 1-AZADIENES | - |
dc.subject.keywordPlus | ALCOHOLS | - |
dc.subject.keywordPlus | OXIMES | - |
dc.subject.keywordPlus | MILD | - |
dc.subject.keywordAuthor | Cascade Reactions | - |
dc.subject.keywordAuthor | Cycloaddition | - |
dc.subject.keywordAuthor | Diels-Alder Reaction | - |
dc.subject.keywordAuthor | Stille Cross-Coupling | - |
dc.subject.keywordAuthor | Total Synthesis | - |
dc.identifier.url | https://onlinelibrary.wiley.com/doi/10.1002/anie.202212016 | - |
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