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- Bielawski, Christopher W.
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| DC Field | Value | Language |
|---|---|---|
| dc.citation.endPage | 4960 | - |
| dc.citation.number | 39 | - |
| dc.citation.startPage | 4958 | - |
| dc.citation.title | CHEMICAL COMMUNICATIONS | - |
| dc.contributor.author | Khramov, DM | - |
| dc.contributor.author | Bielawski, CW | - |
| dc.date.accessioned | 2023-12-22T10:39:28Z | - |
| dc.date.available | 2023-12-22T10:39:28Z | - |
| dc.date.created | 2020-07-13 | - |
| dc.date.issued | 2005 | - |
| dc.description.abstract | Treatment of N-heterocyclic carbenes (as their free carbenes or generated in situ) with alkyl, aryl, acyl or tosyl azides afforded the respective substituted triazenes in excellent yields. | - |
| dc.identifier.bibliographicCitation | CHEMICAL COMMUNICATIONS, no.39, pp.4958 - 4960 | - |
| dc.identifier.doi | 10.1039/b508679e | - |
| dc.identifier.issn | 1359-7345 | - |
| dc.identifier.scopusid | 2-s2.0-27444443660 | - |
| dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/33060 | - |
| dc.identifier.url | https://pubs.rsc.org/en/content/articlelanding/2005/CC/b508679e#!divAbstract | - |
| dc.identifier.wosid | 000232307800022 | - |
| dc.language | 영어 | - |
| dc.publisher | ROYAL SOC CHEMISTRY | - |
| dc.title | Triazene formation via reaction of imidazol-2-ylidenes with azides | - |
| dc.type | Article | - |
| dc.description.isOpenAccess | FALSE | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.type.docType | Article | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.subject.keywordPlus | X-RAY CRYSTAL | - |
| dc.subject.keywordPlus | TOOL | - |
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