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Enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes catalyzed by binaphthyl-derived organocatalysts
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Woo, Saet Byeol | - |
| dc.contributor.author | Kim, Dae Young | - |
| dc.date.accessioned | 2021-08-12T03:25:55Z | - |
| dc.date.available | 2021-08-12T03:25:55Z | - |
| dc.date.issued | 2012-05-07 | - |
| dc.identifier.issn | 1860-5397 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/15171 | - |
| dc.description.abstract | The highly enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes, promoted by binaphthyl-modified chiral bifunctional organocatalysts is described. This reaction afforded the chiral functionalized naphthoquinones in high yields (81-95%) and excellent enantioselectivities (91-98% ee) under low catalyst loading (1 mol %). | - |
| dc.format.extent | 6 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Beilstein-Institut | - |
| dc.title | Enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinones to nitroalkenes catalyzed by binaphthyl-derived organocatalysts | - |
| dc.type | Article | - |
| dc.publisher.location | 독일 | - |
| dc.identifier.doi | 10.3762/bjoc.8.78 | - |
| dc.identifier.scopusid | 2-s2.0-84861112892 | - |
| dc.identifier.wosid | 000303798800001 | - |
| dc.identifier.bibliographicCitation | Beilstein Journal of Organic Chemistry, v.8, pp 699 - 704 | - |
| dc.citation.title | Beilstein Journal of Organic Chemistry | - |
| dc.citation.volume | 8 | - |
| dc.citation.startPage | 699 | - |
| dc.citation.endPage | 704 | - |
| 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 | CONJUGATE ADDITION | - |
| dc.subject.keywordPlus | BETA-KETOESTERS | - |
| dc.subject.keywordPlus | ALPHA,BETA-UNSATURATED KETONES | - |
| dc.subject.keywordPlus | QUATERNARY STEREOCENTERS | - |
| dc.subject.keywordPlus | 1,3-DICARBONYL COMPOUNDS | - |
| dc.subject.keywordPlus | CYTOTOXIC EVALUATION | - |
| dc.subject.keywordPlus | DERIVATIVES | - |
| dc.subject.keywordPlus | CONSTRUCTION | - |
| dc.subject.keywordPlus | DESIGN | - |
| dc.subject.keywordPlus | ALKYLATION | - |
| dc.subject.keywordAuthor | asymmetric catalysis | - |
| dc.subject.keywordAuthor | Michael addition | - |
| dc.subject.keywordAuthor | 1,4-naphthoquinones | - |
| dc.subject.keywordAuthor | nitroalkenes | - |
| dc.subject.keywordAuthor | organocatalysis | - |
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Related Researcher
- Kim, Dae Young
- College of Natural Sciences (Department of Chemistry)