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dc.contributor.author Cho, Soohong -
dc.contributor.author Lee, Yeonjoo -
dc.contributor.author Lee, Kyeongmin -
dc.contributor.author Lee, Hwiwoong -
dc.contributor.author Lee, Yunmi -
dc.contributor.author Jung, Byunghyuck -
dc.date.accessioned 2021-12-29T03:30:01Z -
dc.date.available 2021-12-29T03:30:01Z -
dc.date.created 2021-12-20 -
dc.date.issued 2021-12 -
dc.identifier.issn 1477-0520 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/15987 -
dc.description.abstract An efficient and facile method for the preparation of alkynamides through Et3N-catalyzed alumination of alkyl- or aryl-substituted terminal alkynes with AlMe3and sequential nucleophilic addition ofin situgenerated alkynylaluminums to isocyanates is described. This method has the merits of using readily available isocyanates and monosubstituted alkynes, easy access to organoaluminums, short reaction times, and high efficiency. A gram-scale synthesis of the desired alkynamide and its application to the formation of α-methylene-β-lactams demonstrates the synthetic utility of this method. © The Royal Society of Chemistry 2021. -
dc.language English -
dc.publisher Royal Society of Chemistry -
dc.title Synthesis of alkynamides through reaction of alkyl- or aryl-substituted alkynylaluminums with isocyanates -
dc.type Article -
dc.identifier.doi 10.1039/d1ob01990b -
dc.identifier.wosid 000727427400001 -
dc.identifier.scopusid 2-s2.0-85121720324 -
dc.identifier.bibliographicCitation Organic & Biomolecular Chemistry, v.20, no.1, pp.139 - 151 -
dc.description.isOpenAccess FALSE -
dc.subject.keywordPlus FORMAMIDES -
dc.subject.keywordPlus RESISTANCE -
dc.subject.keywordPlus BETA-LACTAM ANTIBIOTICS -
dc.subject.keywordPlus TERMINAL ALKYNES -
dc.subject.keywordPlus OXIDATIVE AMINOCARBONYLATION -
dc.subject.keywordPlus EFFICIENT SYNTHESIS -
dc.subject.keywordPlus REAGENTS -
dc.subject.keywordPlus AMIDES -
dc.subject.keywordPlus AMINES -
dc.subject.keywordPlus ACIDS -
dc.citation.endPage 151 -
dc.citation.number 1 -
dc.citation.startPage 139 -
dc.citation.title Organic & Biomolecular Chemistry -
dc.citation.volume 20 -
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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Department of Physics and Chemistry Asymmetric Organic Synthesis and Drug Synthesis Laboratory 1. Journal Articles

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