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dc.contributor.authorOzturk, Gulsen
dc.contributor.authorColak, Mehmet
dc.contributor.authorDemirel, Nadir
dc.date.accessioned2019-11-24T20:38:47Z
dc.date.available2019-11-24T20:38:47Z
dc.date.issued2011
dc.identifier.issn0899-0042
dc.identifier.urihttps://dx.doi.org/10.1002/chir.20934
dc.identifier.urihttps://hdl.handle.net/20.500.12513/2577
dc.descriptionWOS: 000289635300002en_US
dc.descriptionPubMed ID: 21488104en_US
dc.description.abstractChiral Schiff-bases 3a-f based on ferrocene were designed and synthesized using solvent-free methods by mixing ferrocene carbaldehyde 1 with amino alcohols and amines 2a-f under microwave irradiation and classical method for the enantioselective nitroaldol (Henry) reaction. The Schiff-bases were obtained in shorter reaction times and improved yield under microwave irradiation method over classical method. The highest enantioselectivity was observed in ligand 3e (95% ee) when CH(2)Cl(2) was used as solvent. Chirality 23: 374-378, 2011. (c) 2011 Wiley-Liss, Inc.en_US
dc.language.isoengen_US
dc.publisherWILEY-BLACKWELLen_US
dc.relation.isversionof10.1002/chir.20934en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectferroceneen_US
dc.subjectmicrowave irradiationen_US
dc.subjectchiral Schiff-basesen_US
dc.subjectnitro aldol reactionen_US
dc.subjectHenry reactionen_US
dc.titleSolvent-Free Synthesis of Chiral Schiff-Base Ligands Based on Ferrocene under Microwave Irradiation and Application to Enantioselective Nitroaldol (Henry) Reactionen_US
dc.typearticleen_US
dc.relation.journalCHIRALITYen_US
dc.contributor.departmentKırşehir Ahi Evran Üniversitesi, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.identifier.volume23en_US
dc.identifier.issue5en_US
dc.identifier.startpage374en_US
dc.identifier.endpage378en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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