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dc.contributor.advisorÇağır, Alien
dc.contributor.authorKayar, Burcuen
dc.date.accessioned2014-07-22T13:51:44Z
dc.date.available2014-07-22T13:51:44Z
dc.date.issued2012en
dc.identifier.urihttp://hdl.handle.net/11147/3532
dc.descriptionThesis (Master)--İzmir Institute of Technology, Chemistry, İzmir, 2012en
dc.descriptionIncludes bibliographical references (leaves: 44-49)en
dc.descriptionText in English; Abstract: Turkish and Englishen
dc.descriptionxi, 72 leavesen
dc.descriptionFull text release delayed at author's request until 2016.01.30en
dc.description.abstractIn last decades, biologically active natural compound (R)-goniothalamin and its derivatives received great attention from researchers. The reason for this interest is the wide range of biological properties of goniothalamin; including anti-microbial, antiprotozoan, anti-inflammatory, cytotoxic and anti-proliferative activities. The present study sets out the asymmetric large scale synthesis of α,β- unsaturated lactone derivative (R)-(+)-6-(2-Methylnaphthalen-1-yl)-5,6-dihydro-2Hpyran- 2-one. In recent studies, this linker modified analog of goniothalamin was shown to be cytotoxic against PC-3 (prostate cancer) and MCF-7 (human breast cancer) cell lines with half maximal inhibitory concentration values of 0.13 μM and 2.6 μM, respectively. The preparation of the target compound consists of three steps. First, asymmetric synthesis of homoallylic alcohol using (R)-Tol-BINAP AgF catalyst complex was performed with allyltrimethoysilane. After that, treating the chiral homoallylic alcohol with acryloylchloride in the presence of triethylamine followed by ring closing metathesis of acrylate ester using 1st generation Grubbs' catalyst finally yielded the lead compound. The large scale preparation of (R)-(+)-6-(2- Methylnaphthalen-1-yl)-5,6-dihydro-2H-pyran-2-one was achieved in order to evaluate its in-vivo anti-cancer activity in mice, and to study its mechanism of action in the cell. Additionally, synthesis of three new 7-membered β-ï § unsaturated lactone derivatives was carried out. Allylation reaction of corresponding aldehydes with allyltrimethoxysilane using CuCl-TBAT gave the racemic homoallylic alcohols. Coupling reactions of this homoallylic alcohol with 3-butenoic acid in the presence of DCC/DMAP yilded the esters. Ring closing metathesis of the related esters was studied by using 2nd generation Grubbs' catalyst.en
dc.language.isoengen
dc.publisherİzmir Institute of Technologyen
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subject.lcshLactones--Synthesisen
dc.titleSynthesis of novel 6,7-dihydro-5h-oxepin-2-one derivativesen
dc.typemasterThesisen
dc.contributor.departmentİzmir Institute of Technology. Chemistryen
dc.relation.publicationcategoryTezen_US


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