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- Park, Cheol-Min
- Synthetic and Medicinal Chemistry Lab.
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| DC Field | Value | Language |
|---|---|---|
| dc.citation.endPage | 7967 | - |
| dc.citation.number | 43 | - |
| dc.citation.startPage | 7963 | - |
| dc.citation.title | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | - |
| dc.citation.volume | 49 | - |
| dc.contributor.author | Lourdusamy, Emmanuvel | - |
| dc.contributor.author | Yao, Lin | - |
| dc.contributor.author | Park, Cheol-Min | - |
| dc.date.accessioned | 2023-12-22T06:42:30Z | - |
| dc.date.available | 2023-12-22T06:42:30Z | - |
| dc.date.created | 2014-11-10 | - |
| dc.date.issued | 2010-10 | - |
| dc.description.abstract | The stereoselective diazo transfer reaction with oxime ethers offers an efficient route to the corresponding α-diazo oxime ethers. The utility of these compounds has been demonstrated by the synthesis of highly substituted pyrroles through a [3+2] cycloaddition of α-oximino carbenoids with enamines (see scheme). | - |
| dc.identifier.bibliographicCitation | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.49, no.43, pp.7963 - 7967 | - |
| dc.identifier.doi | 10.1002/anie.201004073 | - |
| dc.identifier.issn | 1433-7851 | - |
| dc.identifier.scopusid | 2-s2.0-78349243665 | - |
| dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/8542 | - |
| dc.identifier.url | http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=78349243665 | - |
| dc.identifier.wosid | 000283818600025 | - |
| dc.language | 영어 | - |
| dc.publisher | WILEY-V C H VERLAG GMBH | - |
| dc.title | Stereoselective Synthesis of alpha-Diazo Oxime Ethers and Their Application in the Synthesis of Highly Substituted Pyrroles through a [3+2] Cycloaddition | - |
| dc.type | Article | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
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