English

dc.contributor.authorKaranfil, A
dc.contributor.authorEskici, M
dc.date.accessioned2024-07-18T11:56:37Z
dc.date.available2024-07-18T11:56:37Z
dc.description.abstractTAYLOR & FRANCIS INC
dc.identifier.issn1532-2432
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/6789
dc.language.isoArticle
dc.publisher0039-7911
dc.subjectPractical and economical synthesis of synthetically valuable 3,3,3-triethoxypropyne, ketal protected phenyl and methyl substituents prop-2-ynones is described. Bromination and subsequent 18-crown-6 catalyzed elimination of triethylorthoacrylate and ketal protected terminal alkenes with methyl and phenyl substituent which are inturn readily available from triethylorthopropionate, 3-chlorobutan-2-one and propiophenone afforded multigram quantities (>10g) of corresponding functionalized terminal alkynes. Exploration of the synthetic utility of these alkynes is also demonstrated by the acetylenic substitution of the phenylalaninol derived 1,2-cyclic sulfamidate to deliver chiral alkynylated amines. [GRAPHICS] .
dc.titleEnglish
dc.typePROPIOLATE
dc.typeREACTIVITY
dc.typeACETYLIDES

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