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The Giese reaction of alkyl bromides using amine carboxyboranes
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dc.contributor.author Park, Changhee -
dc.contributor.author Gi, Seyun -
dc.contributor.author Yoon, Seongkyeong -
dc.contributor.author Kwon, Seong Jung -
dc.contributor.author Lee, Sunggi -
dc.date.accessioned 2025-04-01T14:10:12Z -
dc.date.available 2025-04-01T14:10:12Z -
dc.date.created 2025-01-31 -
dc.date.issued 2025-03 -
dc.identifier.issn 2052-4110 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/58204 -
dc.description.abstract Amine carboxyborane enabled efficient halogen atom transfer (XAT) with 1 degrees, 2 degrees, and 3 degrees alkyl bromides, resulting in Giese addition products with various electron-deficient double bonds. Moreover, direct addition of several boryl radicals was also possible using several ligated carboxyboranes. -
dc.language English -
dc.publisher Royal Society of Chemistry -
dc.title The Giese reaction of alkyl bromides using amine carboxyboranes -
dc.type Article -
dc.identifier.doi 10.1039/d4qo02325k -
dc.identifier.wosid 001397556700001 -
dc.identifier.scopusid 2-s2.0-85215375790 -
dc.identifier.bibliographicCitation Park, Changhee. (2025-03). The Giese reaction of alkyl bromides using amine carboxyboranes. Organic Chemistry Frontiers, 12(6), 1874–1878. doi: 10.1039/d4qo02325k -
dc.description.isOpenAccess FALSE -
dc.subject.keywordPlus HALOGEN-ATOM TRANSFER -
dc.subject.keywordPlus RADICALS -
dc.subject.keywordPlus HALIDES -
dc.subject.keywordPlus POLARITY-REVERSAL CATALYSIS -
dc.subject.keywordPlus AGENTS -
dc.citation.endPage 1878 -
dc.citation.number 6 -
dc.citation.startPage 1874 -
dc.citation.title Organic Chemistry Frontiers -
dc.citation.volume 12 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Chemistry -
dc.relation.journalWebOfScienceCategory Chemistry, Organic -
dc.type.docType Article -
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