DC Field | Value | Language |
---|---|---|
dc.contributor.author | H S Lee | - |
dc.contributor.author | Sangku Lee | - |
dc.contributor.author | S H Kim | - |
dc.contributor.author | J N Kim | - |
dc.date.accessioned | 2017-04-19T09:25:26Z | - |
dc.date.available | 2017-04-19T09:25:26Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.uri | 10.1016/j.tetlet.2011.07.101 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/10347 | - |
dc.description.abstract | An efficient and regioselective introduction method of 2-methylpyridines to the secondary position of Baylis-Hillman adducts has been developed. A base treatment of 2-methylpyridinium salt of Baylis-Hillman bromide generated N-allylenamine intermediate which underwent a facile 3-aza-Cope rearrangement under mild conditions to produce the product. | - |
dc.publisher | Elsevier | - |
dc.title | Direct one-pot introduction of 2-methylpyridines to Baylis-Hillman adducts via base-mediated 3-aza-Cope rearrangement | - |
dc.title.alternative | Direct one-pot introduction of 2-methylpyridines to Baylis-Hillman adducts via base-mediated 3-aza-Cope rearrangement | - |
dc.type | Article | - |
dc.citation.title | Tetrahedron Letters | - |
dc.citation.number | 39 | - |
dc.citation.endPage | 5042 | - |
dc.citation.startPage | 5039 | - |
dc.citation.volume | 52 | - |
dc.contributor.affiliatedAuthor | Sangku Lee | - |
dc.contributor.alternativeName | 이현승 | - |
dc.contributor.alternativeName | 이상구 | - |
dc.contributor.alternativeName | 김세희 | - |
dc.contributor.alternativeName | 김재녕 | - |
dc.identifier.bibliographicCitation | Tetrahedron Letters, vol. 52, no. 39, pp. 5039-5042 | - |
dc.identifier.doi | 10.1016/j.tetlet.2011.07.101 | - |
dc.subject.keyword | 2-Methylpyridines | - |
dc.subject.keyword | Aza-Cope rearrangement | - |
dc.subject.keyword | Baylis-Hillman adducts | - |
dc.subject.local | 2-Methylpyridines | - |
dc.subject.local | Aza-Cope rearrangement | - |
dc.subject.local | Baylis-Hillman adducts | - |
dc.subject.local | baylis-hillman adducts | - |
dc.description.journalClass | Y | - |
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