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 |
- |