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- Bae, Han Yong
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| DC Field | Value | Language |
|---|---|---|
| dc.citation.endPage | 9623 | - |
| dc.citation.number | 34 | - |
| dc.citation.startPage | 9621 | - |
| dc.citation.title | CHEMICAL COMMUNICATIONS | - |
| dc.citation.volume | 47 | - |
| dc.contributor.author | Bae, Han Yong | - |
| dc.contributor.author | Some, Surajit | - |
| dc.contributor.author | Oh, Joong Suk | - |
| dc.contributor.author | Lee, Yong Seop | - |
| dc.contributor.author | Song, Choong Eui | - |
| dc.date.accessioned | 2023-12-22T05:45:26Z | - |
| dc.date.available | 2023-12-22T05:45:26Z | - |
| dc.date.created | 2019-02-11 | - |
| dc.date.issued | 2011-09 | - |
| dc.description.abstract | Brine provides remarkable rate acceleration and a higher level of stereoselectivity over organic solvents, due to the hydrophobic hydration effect, in the enantioselective Michael addition reactions of 1,3-dicarbonyls to beta-nitroolefins using chiral H-donors as organocatalysts. | - |
| dc.identifier.bibliographicCitation | CHEMICAL COMMUNICATIONS, v.47, no.34, pp.9621 - 9623 | - |
| dc.identifier.doi | 10.1039/c1cc13637b | - |
| dc.identifier.issn | 1359-7345 | - |
| dc.identifier.scopusid | 2-s2.0-80051756054 | - |
| dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/25861 | - |
| dc.identifier.url | https://pubs.rsc.org/en/Content/ArticleLanding/2011/CC/c1cc13637b#!divAbstract | - |
| dc.identifier.wosid | 000293858700015 | - |
| dc.language | 영어 | - |
| dc.publisher | ROYAL SOC CHEMISTRY | - |
| dc.title | Hydrogen bonding mediated enantioselective organocatalysis in brine: significant rate acceleration and enhanced stereoselectivity in enantioselective Michael addition reactions of 1,3-dicarbonyls to beta-nitroolefins | - |
| dc.type | Article | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.subject.keywordPlus | WATER | - |
| dc.subject.keywordPlus | DERIVATIVES | - |
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