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One-Pot Synthesis of 1-Amido-2-cyclohexene Derivatives Catalysed by Ionic Liquids under Solvent-Free Conditions

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dc.date.accessioned 2013-08-14T10:20:28Z und
dc.date.accessioned 2017-10-24T12:19:39Z
dc.date.available 2013-08-14T10:20:28Z und
dc.date.available 2017-10-24T12:19:39Z
dc.date.issued 2013-08-14T10:20:28Z
dc.identifier.uri http://radr.hulib.helsinki.fi/handle/10138.1/3050 und
dc.identifier.uri http://hdl.handle.net/10138.1/3050
dc.title One-Pot Synthesis of 1-Amido-2-cyclohexene Derivatives Catalysed by Ionic Liquids under Solvent-Free Conditions en
ethesis.discipline Organic chemistry en
ethesis.discipline Orgaaninen kemia fi
ethesis.discipline Organisk kemi sv
ethesis.department.URI http://data.hulib.helsinki.fi/id/c2dd677c-da9c-4011-94b0-27b1585ac1cb
ethesis.department Kemiska institutionen sv
ethesis.department Department of Chemistry en
ethesis.department Kemian laitos fi
ethesis.faculty Matematisk-naturvetenskapliga fakulteten sv
ethesis.faculty Matemaattis-luonnontieteellinen tiedekunta fi
ethesis.faculty Faculty of Science en
ethesis.faculty.URI http://data.hulib.helsinki.fi/id/8d59209f-6614-4edd-9744-1ebdaf1d13ca
ethesis.university.URI http://data.hulib.helsinki.fi/id/50ae46d8-7ba9-4821-877c-c994c78b0d97
ethesis.university Helsingfors universitet sv
ethesis.university University of Helsinki en
ethesis.university Helsingin yliopisto fi
dct.creator Debraise, Nora
dct.issued 2013
dct.language.ISO639-2 eng
dct.abstract Aminodiene-based Diels-Alder reactions constitute attractive solutions for the construction of six-membered carbocyclic subunits of a number of organic compounds, including natural products. Functionalized acylaminodienes are key intermediates in those reactions with their ability to incorporate various heteroatoms to the Diels-Alder adducts. Taking advantage of this, various 1-acylamino-2-cyclohexene derivatives were synthesised with a novel protocol involving an in situ generation of an amidodiene intermediate. A novel one-pot procedure for the multicomponent coupling reactions of amides, aldehydes, and dienophiles using room temperature ionic liquids as reaction media and catalyst under solvent-free conditions was developed. Short reaction times, easy microwave-assisted procedure, solvent-free conditions and good conversion to product are features of this new protocol. en
dct.language en
ethesis.language.URI http://data.hulib.helsinki.fi/id/languages/eng
ethesis.language English en
ethesis.language englanti fi
ethesis.language engelska sv
ethesis.thesistype pro gradu-avhandlingar sv
ethesis.thesistype pro gradu -tutkielmat fi
ethesis.thesistype master's thesis en
ethesis.thesistype.URI http://data.hulib.helsinki.fi/id/thesistypes/mastersthesis
dct.identifier.urn URN:NBN:fi-fe2017112252008
dc.type.dcmitype Text

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