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DC Field | Value | Language |
---|---|---|
dc.citation.endPage | 11246 | - |
dc.citation.number | 91 | - |
dc.citation.startPage | 11244 | - |
dc.citation.title | CHEMICAL COMMUNICATIONS | - |
dc.citation.volume | 48 | - |
dc.contributor.author | Qi, Xinxin | - |
dc.contributor.author | Dai, Lu | - |
dc.contributor.author | Park, Cheol-Min | - |
dc.date.accessioned | 2023-12-22T04:39:47Z | - |
dc.date.available | 2023-12-22T04:39:47Z | - |
dc.date.created | 2014-11-10 | - |
dc.date.issued | 2012-10 | - |
dc.description.abstract | Highly efficient synthesis of 3-hydroxypyridines has been developed based on carbenoid-mediated N-O bond insertion. Treatment of δ-diazo oxime ethers with dirhodium complex Rh2(tfacam)4 rapidly provides a variety of pyridines in 5-10 minutes in good to excellent yields. | - |
dc.identifier.bibliographicCitation | CHEMICAL COMMUNICATIONS, v.48, no.91, pp.11244 - 11246 | - |
dc.identifier.doi | 10.1039/c2cc36009h | - |
dc.identifier.issn | 1359-7345 | - |
dc.identifier.scopusid | 2-s2.0-84868028814 | - |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/8486 | - |
dc.identifier.url | http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84868028814 | - |
dc.identifier.wosid | 000310068800024 | - |
dc.language | 영어 | - |
dc.publisher | ROYAL SOC CHEMISTRY | - |
dc.title | Carbenoid-mediated N-O bond insertion and its application in the synthesis of pyridines | - |
dc.type | Article | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | DE-NOVO SYNTHESIS | - |
dc.subject.keywordPlus | DIELS-ALDER REACTION | - |
dc.subject.keywordPlus | ONE-POT SYNTHESIS | - |
dc.subject.keywordPlus | DERIVATIVES | - |
dc.subject.keywordPlus | CYCLOADDITION | - |
dc.subject.keywordPlus | ALKYNES | - |
dc.subject.keywordPlus | 1,2,4-TRIAZINES | - |
dc.subject.keywordPlus | ISOQUINOLINES | - |
dc.subject.keywordPlus | CYCLIZATION | - |
dc.subject.keywordPlus | ACETYLENES | - |
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