DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kang, Sungkyoung | ko |
dc.contributor.author | Lee, Wonchul | ko |
dc.contributor.author | Jung, Byunghyuck | ko |
dc.contributor.author | Lee, Hee-Seung | ko |
dc.contributor.author | Kang, Sung-Ho | ko |
dc.date.accessioned | 2015-07-21T04:47:23Z | - |
dc.date.available | 2015-07-21T04:47:23Z | - |
dc.date.created | 2015-06-30 | - |
dc.date.created | 2015-06-30 | - |
dc.date.created | 2015-06-30 | - |
dc.date.issued | 2015-06 | - |
dc.identifier.citation | ASIAN JOURNAL OF ORGANIC CHEMISTRY, v.4, no.6, pp.567 - 572 | - |
dc.identifier.issn | 2193-5807 | - |
dc.identifier.uri | http://hdl.handle.net/10203/199775 | - |
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. | - |
dc.language | English | - |
dc.publisher | WILEY-V C H VERLAG GMBH | - |
dc.title | Stereocontrolled Synthesis of the C1-C10 Fragments of Monensin B and Laidlomycin | - |
dc.type | Article | - |
dc.identifier.wosid | 000355651000011 | - |
dc.identifier.scopusid | 2-s2.0-84930177897 | - |
dc.type.rims | ART | - |
dc.citation.volume | 4 | - |
dc.citation.issue | 6 | - |
dc.citation.beginningpage | 567 | - |
dc.citation.endingpage | 572 | - |
dc.citation.publicationname | ASIAN JOURNAL OF ORGANIC CHEMISTRY | - |
dc.identifier.doi | 10.1002/ajoc.201500078 | - |
dc.contributor.localauthor | Lee, Hee-Seung | - |
dc.contributor.localauthor | Kang, Sung-Ho | - |
dc.contributor.nonIdAuthor | Lee, Wonchul | - |
dc.contributor.nonIdAuthor | Jung, Byunghyuck | - |
dc.description.isOpenAccess | N | - |
dc.type.journalArticle | Article | - |
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 | POLYETHER IONOPHORE ANTIBIOTICS | - |
dc.subject.keywordPlus | MEDIATED GROWTH-INHIBITION | - |
dc.subject.keywordPlus | CELL-CYCLE ARREST | - |
dc.subject.keywordPlus | CONVERGENT SYNTHESIS | - |
dc.subject.keywordPlus | CLAISEN REARRANGEMENT | - |
dc.subject.keywordPlus | MOLECULAR-STRUCTURE | - |
dc.subject.keywordPlus | ESTER ENOLATE | - |
dc.subject.keywordPlus | LEAVING GROUP | - |
dc.subject.keywordPlus | APOPTOSIS | - |
dc.subject.keywordPlus | COMPLEX | - |
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