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Stereoselective One-Pot Synthesis of 1-Aminoindanes and 5,6 Fused Azacycles Using a Gold-Catalyzed Redox-Pinacol-Mannich-Michael Cascade
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Yeom, Hyun-Suk | - |
| dc.contributor.author | Lee, Youngun | - |
| dc.contributor.author | Jeong, Jaewon | - |
| dc.contributor.author | So, Eunsoo | - |
| dc.contributor.author | Hwang, Soojin | - |
| dc.contributor.author | Lee, Ji-Eun | - |
| dc.contributor.author | Lee, Shim Sung | - |
| dc.contributor.author | Shin, Seunghoon | - |
| dc.date.accessioned | 2022-12-20T19:02:28Z | - |
| dc.date.available | 2022-12-20T19:02:28Z | - |
| dc.date.created | 2022-08-27 | - |
| dc.date.issued | 2010-02 | - |
| dc.identifier.issn | 1433-7851 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/175472 | - |
| dc.description.abstract | "Chemical Equation Presented" Just another Mannich Monday: A cascade intramolecular redox-pinacol-Mannich-Michael reaction sequence catalyzed by gold complexes can be used to generate a variety of structures including spirocycles, 1-aminoindanes, and 5,6-fused azabicycles that have a quaternary carbon center. The reaction is characterized by complete atom-economy, high diastereoselectivity, and remarkable efficiency through tandem reactions. | - |
| dc.language | 영어 | - |
| dc.language.iso | en | - |
| dc.publisher | WILEY-V C H VERLAG GMBH | - |
| dc.title | Stereoselective One-Pot Synthesis of 1-Aminoindanes and 5,6 Fused Azacycles Using a Gold-Catalyzed Redox-Pinacol-Mannich-Michael Cascade | - |
| dc.type | Article | - |
| dc.contributor.affiliatedAuthor | Shin, Seunghoon | - |
| dc.identifier.doi | 10.1002/anie.200906346 | - |
| dc.identifier.scopusid | 2-s2.0-77649120676 | - |
| dc.identifier.wosid | 000275234800014 | - |
| dc.identifier.bibliographicCitation | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.49, no.9, pp.1611 - 1614 | - |
| dc.relation.isPartOf | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | - |
| dc.citation.title | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | - |
| dc.citation.volume | 49 | - |
| dc.citation.number | 9 | - |
| dc.citation.startPage | 1611 | - |
| dc.citation.endPage | 1614 | - |
| dc.type.rims | ART | - |
| dc.type.docType | Article | - |
| dc.description.journalClass | 1 | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.subject.keywordPlus | TRANSFER HYDROGENATION | - |
| dc.subject.keywordPlus | 3-COMPONENT REACTION | - |
| dc.subject.keywordPlus | CARBONYL-COMPOUNDS | - |
| dc.subject.keywordPlus | ORGANIC-SYNTHESIS | - |
| dc.subject.keywordPlus | TANDEM REACTION | - |
| dc.subject.keywordPlus | AU CATALYSIS | - |
| dc.subject.keywordPlus | PI-ACIDS | - |
| dc.subject.keywordPlus | GENERATION | - |
| dc.subject.keywordPlus | YLIDES | - |
| dc.subject.keywordPlus | CYCLOISOMERIZATION | - |
| dc.subject.keywordAuthor | carbenoids | - |
| dc.subject.keywordAuthor | cascade reactions | - |
| dc.subject.keywordAuthor | gold | - |
| dc.subject.keywordAuthor | Mannich reactions | - |
| dc.subject.keywordAuthor | redox chemistry | - |
| dc.identifier.url | https://onlinelibrary.wiley.com/doi/10.1002/anie.200906346 | - |
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Related Researcher
- Shin, Seung hoon
- COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF CHEMISTRY)