Department of Physics and Chemistry
Asymmetric Organic Synthesis and Drug Synthesis Laboratory
1. Journal Articles
Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kang, Sungkyoung | - |
| dc.contributor.author | Lee, Wonchul | - |
| dc.contributor.author | Jung, Byunghyuck | - |
| dc.contributor.author | Lee, Hee-Seung | - |
| dc.contributor.author | Kang, Sung Ho | - |
| dc.date.accessioned | 2018-01-25T01:10:19Z | - |
| dc.date.available | 2018-01-25T01:10:19Z | - |
| dc.date.created | 2017-04-10 | - |
| dc.date.issued | 2015-06 | - |
| dc.identifier.issn | 2193-5807 | - |
| dc.identifier.uri | http://hdl.handle.net/20.500.11750/5186 | - |
| dc.description.abstract | An efficient synthetic route to the C1-C10 fragments of laidlomycin and monensin B has been developed toward their total synthesis. The asymmetric carbons have been elaborated by a syn-aldol reaction using the oxazolidinone chiral auxiliary for C6 and C7, an anti-aldol reaction for C3 and C4, the Tishchenko-Evans reaction for C5, and a chiral building block for C2. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | - |
| dc.publisher | Wiley-VCH Verlag | - |
| dc.title | Stereocontrolled Synthesis of the C1-C10 Fragments of Monensin B and Laidlomycin | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.1002/ajoc.201500078 | - |
| dc.identifier.scopusid | 2-s2.0-84930177897 | - |
| dc.identifier.bibliographicCitation | Asian Journal of Organic Chemistry, v.4, no.6, pp.567 - 572 | - |
| dc.subject.keywordAuthor | aldol reaction | - |
| dc.subject.keywordAuthor | laidlomycin | - |
| dc.subject.keywordAuthor | monensin B | - |
| dc.subject.keywordAuthor | Tishchenko-Evans reaction | - |
| dc.subject.keywordAuthor | total synthesis | - |
| dc.subject.keywordPlus | Aldol Reaction | - |
| dc.subject.keywordPlus | APOPTOSIS | - |
| dc.subject.keywordPlus | CELL-CYCLE ARREST | - |
| dc.subject.keywordPlus | CLAISEN REARRANGemENT | - |
| dc.subject.keywordPlus | COMPLEX | - |
| dc.subject.keywordPlus | CONVERGENT SYNTHESIS | - |
| dc.subject.keywordPlus | ESTER ENOLATE | - |
| dc.subject.keywordPlus | Laidlomycin | - |
| dc.subject.keywordPlus | LEAVING GROUP | - |
| dc.subject.keywordPlus | MEDIATED GROWTH-INHIBITION | - |
| dc.subject.keywordPlus | MOLECULAR-STRUCTURE | - |
| dc.subject.keywordPlus | Monensin B | - |
| dc.subject.keywordPlus | POLYETHER IONOPHORE ANTIBIOTICS | - |
| dc.subject.keywordPlus | Tishchenko-Evans Reaction | - |
| dc.subject.keywordPlus | Total Synthesis | - |
| dc.citation.endPage | 572 | - |
| dc.citation.number | 6 | - |
| dc.citation.startPage | 567 | - |
| dc.citation.title | Asian Journal of Organic Chemistry | - |
| dc.citation.volume | 4 | - |
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