Synthetic strategies towards the carbenoid reactions of ?, ? -acetylenic carbonyls

dc.contributor.authorKışkan, Füsun Şeyma
dc.contributor.authorÖzgüz, Emre
dc.contributor.authorAnaç, Olcay
dc.contributor.authorTarakçı, Nurdan
dc.contributor.authorMerey, Gökçe
dc.date.accessioned2021-11-01T18:17:58Z
dc.date.available2021-11-01T18:17:58Z
dc.date.issued2018
dc.department[Belirlenecek]
dc.description.abstractCatalytic reactions of ?, ? -conjugated carbonyl compounds have been a practical tool towards the synthesis of different useful heterocyclic compounds. Despite the numerous reactions with carbon-carbon double bond conjugated carbonyls, reactions of acetylenic carbonyls are limited. In this study, efficient dioxole synthesis was carried out via acetylenic aldehydes and butadiene formation was preferred over cyclopropene formation via acetylenic esters as different functional groups on these substrates change the product distribution. Both reaction conditions (such as solvent and temperature) and electrophilic structure of metal carbenoids alter the product distribution; acceptor (A), donor-acceptor (DA), and acceptor-acceptor (AA) functionalized diazo compounds yield different product types over different mechanisms.
dc.identifier.doi10.3906/kim-1805-65
dc.identifier.endpage1397en_US
dc.identifier.issn1300-0527
dc.identifier.issn1303-6130
dc.identifier.issue5en_US
dc.identifier.startpage1384en_US
dc.identifier.urihttps://doi.org10.3906/kim-1805-65
dc.identifier.urihttps://app.trdizin.gov.tr/makale/TXpneE5qazVPUT09
dc.identifier.urihttps://hdl.handle.net/11491/7816
dc.identifier.volume42en_US
dc.indekslendigikaynakTR-Dizin
dc.institutionauthor[Belirlenecek]
dc.language.isoen
dc.relation.ispartofTurkish Journal of Chemistry
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject[No Keywords]en_US
dc.titleSynthetic strategies towards the carbenoid reactions of ?, ? -acetylenic carbonyls
dc.typeArticle

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