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Site-Specific Synthesis of Carbazole Derivatives through Aryl Homocoupling and Amination
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Ban, Jaeyoung | - |
| dc.contributor.author | Lim, Minkyung | - |
| dc.contributor.author | Shabbir, Saira | - |
| dc.contributor.author | Baek, Junghyun | - |
| dc.contributor.author | Rhee, Hakjune | - |
| dc.date.accessioned | 2021-06-22T09:06:45Z | - |
| dc.date.available | 2021-06-22T09:06:45Z | - |
| dc.date.issued | 2020-03 | - |
| dc.identifier.issn | 0039-7881 | - |
| dc.identifier.issn | 1437-210X | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/1214 | - |
| dc.description.abstract | We synthesized various carbazoles from anilines through a three-step process with good overall yields (up to 48%). This process comprises N-acetylation, copper(0)-mediated Ullmann homocoupling, and acid-mediated intramolecular amination. It permits various functional-groups on the substrate. Scale-up of the developed three-step synthetic route to carbazoles was also demonstrated. | - |
| dc.format.extent | 11 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Georg Thieme Verlag | - |
| dc.title | Site-Specific Synthesis of Carbazole Derivatives through Aryl Homocoupling and Amination | - |
| dc.type | Article | - |
| dc.publisher.location | 독일 | - |
| dc.identifier.doi | 10.1055/s-0039-1690759 | - |
| dc.identifier.scopusid | 2-s2.0-85081231768 | - |
| dc.identifier.wosid | 000519236300014 | - |
| dc.identifier.bibliographicCitation | Synthesis, v.52, no.6, pp 917 - 927 | - |
| dc.citation.title | Synthesis | - |
| dc.citation.volume | 52 | - |
| dc.citation.number | 6 | - |
| dc.citation.startPage | 917 | - |
| dc.citation.endPage | 927 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.subject.keywordPlus | C-H AMINATION | - |
| dc.subject.keywordPlus | HIGH TRIPLET ENERGY | - |
| dc.subject.keywordPlus | HOST MATERIALS | - |
| dc.subject.keywordPlus | PALLADIUM | - |
| dc.subject.keywordPlus | ANILIDES | - |
| dc.subject.keywordPlus | HALOGENATION | - |
| dc.subject.keywordPlus | IODINATION | - |
| dc.subject.keywordPlus | ACTIVATION | - |
| dc.subject.keywordPlus | CATALYST | - |
| dc.subject.keywordPlus | UTILITY | - |
| dc.subject.keywordAuthor | N-acetylation | - |
| dc.subject.keywordAuthor | aryl homocoupling | - |
| dc.subject.keywordAuthor | Ullmann coupling reaction | - |
| dc.subject.keywordAuthor | Tauber carbazole synthesis | - |
| dc.subject.keywordAuthor | intramolecular amination | - |
| dc.identifier.url | https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0039-1690759 | - |
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Related Researcher
- Rhee, Hak june
- ERICA 공학대학 (ERICA 에너지바이오학과)