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- Park, Cheol-Min
- Synthetic and Medicinal Chemistry Lab.
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| DC Field | Value | Language |
|---|---|---|
| dc.citation.endPage | 3435 | - |
| dc.citation.number | 13 | - |
| dc.citation.startPage | 3432 | - |
| dc.citation.title | ORGANIC LETTERS | - |
| dc.citation.volume | 16 | - |
| dc.contributor.author | Jiang, Yaojia | - |
| dc.contributor.author | Park, Cheol-Min | - |
| dc.contributor.author | Loh, Teck-Peng | - |
| dc.date.accessioned | 2023-12-22T02:37:03Z | - |
| dc.date.available | 2023-12-22T02:37:03Z | - |
| dc.date.created | 2014-07-30 | - |
| dc.date.issued | 2014-07 | - |
| dc.description.abstract | A new strategy to open the 2-allyl-2H-azirines by 1,8-diazabicyclo[5.4.0] undec-7-ene (DBU) promotion in metal-free conditions affording 1-azatrienes that in situ electrocyclize to the pyridines in good to excellent yields is reported. The reaction displays a broad substrate scope and good tolerance to a variety of substituents including aryl, alkyl, and heterocyclic groups. In addition, one-pot synthesis of pyridines from oximes via in situ formation of 2H-azirines was achieved. | - |
| dc.identifier.bibliographicCitation | ORGANIC LETTERS, v.16, no.13, pp.3432 - 3435 | - |
| dc.identifier.doi | 10.1021/ol501010k | - |
| dc.identifier.issn | 1523-7060 | - |
| dc.identifier.scopusid | 2-s2.0-84903689092 | - |
| dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/5276 | - |
| dc.identifier.url | http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84903689092 | - |
| dc.identifier.wosid | 000340808000004 | - |
| dc.language | 영어 | - |
| dc.publisher | AMER CHEMICAL SOC | - |
| dc.title | Transition-metal-free synthesis of substituted pyridines via ring expansion of 2-allyl-2H-azirines | - |
| dc.type | Article | - |
| dc.description.isOpenAccess | FALSE | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
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