Electrochemical oxidative bromolactonization of unsaturated carboxylic acids with sodium bromide: Synthesis of bromomethylated gamma-lactones
DC Field | Value | Language |
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dc.contributor.author | Kim, Rabin | - |
dc.contributor.author | Ha, Jeauk | - |
dc.contributor.author | Woo, Jiwon | - |
dc.contributor.author | Kim, Dae Young | - |
dc.date.accessioned | 2022-01-20T09:40:10Z | - |
dc.date.available | 2022-01-20T09:40:10Z | - |
dc.date.issued | 2022-01-05 | - |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/20198 | - |
dc.description.abstract | Electrochemical oxidative bromination and cyclization sequences of unsaturated carboxylic acids were developed in this study. This approach is environmentally-friendly, using bromide anion as bromine radical precursor without external oxidizing reagents. The electrochemical protocol offers a facile way to prepare bromomethylated y-lactones derivatives in moderate to high yields. (c) 2021 Elsevier Ltd. All rights reserved. | - |
dc.format.extent | 5 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Elsevier BV | - |
dc.title | Electrochemical oxidative bromolactonization of unsaturated carboxylic acids with sodium bromide: Synthesis of bromomethylated gamma-lactones | - |
dc.type | Article | - |
dc.publisher.location | 영국 | - |
dc.identifier.doi | 10.1016/j.tetlet.2021.153567 | - |
dc.identifier.scopusid | 2-s2.0-85121142060 | - |
dc.identifier.wosid | 000740353300023 | - |
dc.identifier.bibliographicCitation | Tetrahedron Letters, v.88, no.0, pp 1 - 5 | - |
dc.citation.title | Tetrahedron Letters | - |
dc.citation.volume | 88 | - |
dc.citation.number | 0 | - |
dc.citation.startPage | 1 | - |
dc.citation.endPage | 5 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | C-H FUNCTIONALIZATION | - |
dc.subject.keywordPlus | MIGRATION SEQUENCES | - |
dc.subject.keywordPlus | ALKENOIC ACIDS | - |
dc.subject.keywordPlus | ELECTROCATALYTIC APPROACH | - |
dc.subject.keywordPlus | RING EXPANSION | - |
dc.subject.keywordPlus | QUINOXALIN-2(1H)-ONES | - |
dc.subject.keywordPlus | CYCLOPENTANONES | - |
dc.subject.keywordPlus | HALOCYCLIZATION | - |
dc.subject.keywordPlus | HALOGENATION | - |
dc.subject.keywordPlus | BROMINATION | - |
dc.subject.keywordAuthor | Electrochemical reaction | - |
dc.subject.keywordAuthor | Bromolactonization | - |
dc.subject.keywordAuthor | y -Lactones | - |
dc.subject.keywordAuthor | Anodic oxidation | - |
dc.subject.keywordAuthor | Alkenoic acids | - |
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