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| DC Field | Value | Language |
|---|---|---|
| dc.citation.endPage | 12147 | - |
| dc.citation.number | 46 | - |
| dc.citation.startPage | 12143 | - |
| dc.citation.title | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | - |
| dc.citation.volume | 52 | - |
| dc.contributor.author | Bae, Han Yong | - |
| dc.contributor.author | Sim, Jae Hun | - |
| dc.contributor.author | Lee, Ji-Woong | - |
| dc.contributor.author | List, Benjamin | - |
| dc.contributor.author | Song, Choong Eui | - |
| dc.date.accessioned | 2023-12-22T03:13:01Z | - |
| dc.date.available | 2023-12-22T03:13:01Z | - |
| dc.date.created | 2019-02-11 | - |
| dc.date.issued | 2013-11 | - |
| dc.description.abstract | Copycat: A highly enantioselective biomimetic aldol reaction of malonic acid half thioesters with a variety of aldehydes affords optically active β-hydroxy thioesters by employing the cinchona-derived sulfonamide organocatalyst 1. The synthetic utility of this protocol was demonstrated by performing formal syntheses of the antidepressants (R)-fluoxetine, (R)-tomoxetine, (-)-paroxetine, and (R)-duloxetine. | - |
| dc.identifier.bibliographicCitation | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.52, no.46, pp.12143 - 12147 | - |
| dc.identifier.doi | 10.1002/anie.201306297 | - |
| dc.identifier.issn | 1433-7851 | - |
| dc.identifier.scopusid | 2-s2.0-84887419508 | - |
| dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/25874 | - |
| dc.identifier.url | https://onlinelibrary.wiley.com/doi/full/10.1002/anie.201306297 | - |
| dc.identifier.wosid | 000326670800043 | - |
| dc.language | 영어 | - |
| dc.publisher | WILEY-V C H VERLAG GMBH | - |
| dc.title | Organocatalytic Enantioselective Decarboxylative Aldol Reaction of Malonic Acid Half Thioesters with Aldehydes | - |
| dc.type | Article | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
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