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A practical gold-catalyzed route to 4-substituted oxazolidin-2-ones from N-Boc propargylamines
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, Eun-Sun | - |
| dc.contributor.author | Yeom, Hyun-Suk | - |
| dc.contributor.author | Hwang, Ji-Hyun | - |
| dc.contributor.author | Shin, Seunghoon | - |
| dc.date.accessioned | 2022-12-21T07:18:40Z | - |
| dc.date.available | 2022-12-21T07:18:40Z | - |
| dc.date.issued | 2007-07 | - |
| dc.identifier.issn | 1434-193X | - |
| dc.identifier.issn | 1099-0690 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/179894 | - |
| dc.description.abstract | Au-I-catalyzed cyclization of N-Boc propargylamines into 4-alkylidene oxazolidin-2-ones is described. This modular approach provides access to a variety of nonproteogenic 4-substituted oxazolidinones that are important in asymmetric synthesis and biological applications. The current flexible route is characterized by low catalyst loading, mild conditions, and operational simplicity. | - |
| dc.format.extent | 5 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | John Wiley & Sons Ltd. | - |
| dc.title | A practical gold-catalyzed route to 4-substituted oxazolidin-2-ones from N-Boc propargylamines | - |
| dc.type | Article | - |
| dc.publisher.location | 독일 | - |
| dc.identifier.doi | 10.1002/ejoc.200700210 | - |
| dc.identifier.scopusid | 2-s2.0-34447576888 | - |
| dc.identifier.wosid | 000248232100010 | - |
| dc.identifier.bibliographicCitation | European Journal of Organic Chemistry, v.2007, no.21, pp 3503 - 3507 | - |
| dc.citation.title | European Journal of Organic Chemistry | - |
| dc.citation.volume | 2007 | - |
| dc.citation.number | 21 | - |
| dc.citation.startPage | 3503 | - |
| dc.citation.endPage | 3507 | - |
| 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 | INTRAMOLECULAR HYDROAMINATION | - |
| dc.subject.keywordPlus | GOLD(I)-CATALYZED FORMATION | - |
| dc.subject.keywordPlus | CYTOKINE MODULATOR | - |
| dc.subject.keywordPlus | MILD CONDITIONS | - |
| dc.subject.keywordPlus | BETA-AMINO | - |
| dc.subject.keywordPlus | CYCLIZATION | - |
| dc.subject.keywordPlus | 2-OXAZOLIDINONES | - |
| dc.subject.keywordPlus | OXAZOLIDINONES | - |
| dc.subject.keywordPlus | REAGENTS | - |
| dc.subject.keywordPlus | SULFONES | - |
| dc.subject.keywordAuthor | gold | - |
| dc.subject.keywordAuthor | oxazolidinones | - |
| dc.subject.keywordAuthor | 1,3-allylic interactions | - |
| dc.subject.keywordAuthor | isomerization | - |
| dc.identifier.url | https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.200700210 | - |
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