AgOTf and TfOH co-catalyzed isoquinoline synthesis via redox reactions of O-alkyl oximes
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hwang, Soojin | - |
dc.contributor.author | Lee, Youngun | - |
dc.contributor.author | Lee, Phil Ho | - |
dc.contributor.author | Shin, Seunghoon | - |
dc.date.accessioned | 2022-12-20T22:28:04Z | - |
dc.date.available | 2022-12-20T22:28:04Z | - |
dc.date.created | 2022-08-26 | - |
dc.date.issued | 2009-05 | - |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/176878 | - |
dc.description.abstract | Under AgOTf and Bronsted acid co-catalysis, O-alkyl o-alkynylbenzaldoxime derivatives undergo a cyclization-induced N-O cleavage to produce isoquinolines with the simultaneous oxidation of O-alkyl group. This redox-based method provides a general access to diverse isoquinoline-derived heterocycles that are simple, efficient, and tolerant of various functional groups from readily available and hydrolytically stable oxime precursors. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.title | AgOTf and TfOH co-catalyzed isoquinoline synthesis via redox reactions of O-alkyl oximes | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Shin, Seunghoon | - |
dc.identifier.doi | 10.1016/j.tetlet.2009.02.144 | - |
dc.identifier.scopusid | 2-s2.0-63349092743 | - |
dc.identifier.wosid | 000265517700004 | - |
dc.identifier.bibliographicCitation | TETRAHEDRON LETTERS, v.50, no.20, pp.2305 - 2308 | - |
dc.relation.isPartOf | TETRAHEDRON LETTERS | - |
dc.citation.title | TETRAHEDRON LETTERS | - |
dc.citation.volume | 50 | - |
dc.citation.number | 20 | - |
dc.citation.startPage | 2305 | - |
dc.citation.endPage | 2308 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | HIGHLY EFFICIENT | - |
dc.subject.keywordPlus | CYCLIZATION | - |
dc.subject.keywordPlus | ALDOXIMES | - |
dc.subject.keywordPlus | PYRIDINES | - |
dc.subject.keywordPlus | CYCLOISOMERIZATION | - |
dc.subject.keywordPlus | GENERATION | - |
dc.subject.keywordPlus | IMINES | - |
dc.subject.keywordPlus | ETHERS | - |
dc.subject.keywordPlus | ROUTE | - |
dc.subject.keywordPlus | WATER | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0040403909004134?via%3Dihub | - |
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