Cited 181 time in
Pd-Catalyzed Intramolecular Oxidative C-H Amination: Synthesis of Carbazoles
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Youn, So Won | - |
| dc.contributor.author | Bihn, Joon Hyung | - |
| dc.contributor.author | Kim, Byung Seok | - |
| dc.date.accessioned | 2022-07-07T14:28:43Z | - |
| dc.date.available | 2022-07-07T14:28:43Z | - |
| dc.date.issued | 2011-07 | - |
| dc.identifier.issn | 1523-7060 | - |
| dc.identifier.issn | 1523-7052 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/144878 | - |
| dc.description.abstract | A Pd-catalyzed oxidative C-H amination of N-Ts-2-arylanilines under ambient temperature using Ozone as an inexpensive, safe, and easy-to-handle oxidant has been developed. This process represents a green and practical method for the facile construction of carbazoles with a broad substrate scope and wide functional group tolerance. | - |
| dc.format.extent | 4 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | American Chemical Society | - |
| dc.title | Pd-Catalyzed Intramolecular Oxidative C-H Amination: Synthesis of Carbazoles | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1021/ol201416u | - |
| dc.identifier.scopusid | 2-s2.0-79960166031 | - |
| dc.identifier.wosid | 000292479300048 | - |
| dc.identifier.bibliographicCitation | Organic Letters, v.13, no.14, pp 3738 - 3741 | - |
| dc.citation.title | Organic Letters | - |
| dc.citation.volume | 13 | - |
| dc.citation.number | 14 | - |
| dc.citation.startPage | 3738 | - |
| dc.citation.endPage | 3741 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.subject.keywordPlus | N BOND FORMATION | - |
| dc.subject.keywordPlus | TRANSITION-METAL-COMPLEXES | - |
| dc.subject.keywordPlus | 1ST TOTAL-SYNTHESIS | - |
| dc.subject.keywordPlus | ORGANIC-SYNTHESIS | - |
| dc.subject.keywordPlus | REDUCTIVE ELIMINATION | - |
| dc.subject.keywordPlus | COUPLING REACTIONS | - |
| dc.subject.keywordPlus | DIRECT ARYLATION | - |
| dc.subject.keywordPlus | BIARYL SYNTHESIS | - |
| dc.subject.keywordPlus | PRIMARY AMINES | - |
| dc.subject.keywordPlus | PALLADIUM | - |
| dc.identifier.url | https://pubs.acs.org/doi/10.1021/ol201416u | - |
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