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The first asymmetric synthesis of marliolide from readily accessible carbohydrate as chiral template
Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mailar, Karabasappa | - |
| dc.contributor.author | Choi, Won Jun | - |
| dc.date.accessioned | 2024-09-25T03:00:32Z | - |
| dc.date.available | 2024-09-25T03:00:32Z | - |
| dc.date.issued | 2016-09-02 | - |
| dc.identifier.issn | 0008-6215 | - |
| dc.identifier.issn | 1873-426X | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/23419 | - |
| dc.description.abstract | A simple and efficient strategy for the first asymmetric total synthesis of marliolide was accomplished by using stereoselective alkylation of the dianion of the beta-hydroxy lactone enolate with myristyl aldehyde as a key step. The key intermediate, beta-hydroxyl gamma-methyl butyrolactone was prepared by transformation of L-lyxonolactone starting from D-ribose, a naturally abundant chiral carbohydrate. (C) 2016 Elsevier Ltd. All rights reserved. | - |
| dc.format.extent | 5 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | ELSEVIER SCI LTD | - |
| dc.title | The first asymmetric synthesis of marliolide from readily accessible carbohydrate as chiral template | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1016/j.carres.2016.06.005 | - |
| dc.identifier.scopusid | 2-s2.0-84976258983 | - |
| dc.identifier.wosid | 000380682800005 | - |
| dc.identifier.bibliographicCitation | CARBOHYDRATE RESEARCH, v.432, pp 31 - 35 | - |
| dc.citation.title | CARBOHYDRATE RESEARCH | - |
| dc.citation.volume | 432 | - |
| dc.citation.startPage | 31 | - |
| dc.citation.endPage | 35 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Applied | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.subject.keywordPlus | POTENTIAL TUMOR INHIBITORS | - |
| dc.subject.keywordPlus | LACTONES | - |
| dc.subject.keywordPlus | CYTOTOXICITY | - |
| dc.subject.keywordPlus | DERIVATIVES | - |
| dc.subject.keywordPlus | ALKYLATION | - |
| dc.subject.keywordAuthor | Marliolide | - |
| dc.subject.keywordAuthor | Asymmetric synthesis | - |
| dc.subject.keywordAuthor | gamma-butyrolactone | - |
| dc.subject.keywordAuthor | Lactone enolate alkylation | - |
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Related Researcher
- Choi, Won Jun
- College of Pharmacy (Department of Pharmacy)