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dc.contributor.authorGezegen, Hayreddin
dc.contributor.authorCeylan, Mustafa
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:56:28Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:56:28Z
dc.date.issued2015
dc.identifier.issn0039-7911
dc.identifier.issn1532-2432
dc.identifier.urihttps://dx.doi.org/10.1080/00397911.2015.1080845
dc.identifier.urihttps://hdl.handle.net/20.500.12418/8017
dc.descriptionWOS: 000362369000006en_US
dc.description.abstractA series of novel 1,2,3,4,6-pentasubstituted-4-hydroxy-cyclohexanes (3a-u) were synthesized from the reaction of aromatic ketones with aromatic aldehydes under mild reaction conditions in good yields. The stereochemistry of the synthesized compounds was established using 1D and 2D-NMR spectra.en_US
dc.description.sponsorshipGaziosmanpasa University [BAP-2011/94]en_US
dc.description.sponsorshipThe authors are indebted to Gaziosmanpasa University (Grant BAP-2011/94) for financial support of this work.en_US
dc.language.isoengen_US
dc.publisherTAYLOR & FRANCIS INCen_US
dc.relation.isversionof10.1080/00397911.2015.1080845en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDomino reactionsen_US
dc.subjectone-pot chemoselective synthesisen_US
dc.subjectpentasubstituted cyclohexanolen_US
dc.titleAlternate Method for the Synthesis of Six-Membered Carbocycles with Five Stereocenters: 1,2,3,4,6-Pentasubstituted-4-hydroxy-cyclohexanesen_US
dc.typearticleen_US
dc.relation.journalSYNTHETIC COMMUNICATIONSen_US
dc.contributor.department[Gezegen, Hayreddin] Cumhuriyet Univ, Dept Nutr & Dietet, Fac Hlth Sci, TR-58140 Sivas, Turkey -- [Ceylan, Mustafa] Gaziosmanpasa Univ, Fac Arts & Sci, Dept Chem, Tokat, Turkeyen_US
dc.contributor.authorIDGezegen, Hayreddin -- 0000-0003-3602-7400en_US
dc.identifier.volume45en_US
dc.identifier.issue20en_US
dc.identifier.endpage2349en_US
dc.identifier.startpage2344en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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