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dc.contributor.authorHoff, Bård Helge
dc.date.accessioned2019-05-29T09:10:56Z
dc.date.available2019-05-29T09:10:56Z
dc.date.created2018-12-19T12:29:50Z
dc.date.issued2018
dc.identifier.citationSynthesis (Stuttgart). 2018, 50 (15), 2824-2852.nb_NO
dc.identifier.issn0039-7881
dc.identifier.urihttp://hdl.handle.net/11250/2599396
dc.description.abstractAcetonitrile is popular as a solvent for performing organic reactions, as a ligand in inorganic chemistry, as a mobile phase in chromatography, and as an electrolyte solvent in dye-sensitized solar cells. This is mainly due to its ability to dissolve both polar and nonpolar components. However, acetonitrile is also a valuable building block allowing atom-efficient transformations in synthetic organic chemistry. The aim of this review is to highlight synthetic transformations using acetonitrile, covering both classical approaches and modern strategies proceeding through radical intermediates or mediated by metal catalysis. Besides showcasing synthetic protocols useful for acetonitrile and analogues, warnings for when not to use acetonitrile as a solvent are also provided.nb_NO
dc.language.isoengnb_NO
dc.publisherThieme Publishingnb_NO
dc.titleAcetonitrile as a Building Block and Reactantnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber2824-2852nb_NO
dc.source.volume50nb_NO
dc.source.journalSynthesis (Stuttgart)nb_NO
dc.source.issue15nb_NO
dc.identifier.doi10.1055/s-0036-1589535
dc.identifier.cristin1645566
dc.description.localcode© Thieme Publishing Group 2018. This is the authors accepted and refereed manuscript to the article. Locked until 13.6.2019 due to copyright restrictions. Available at http://dx.doi.org/10.1055/s-0036-1589535nb_NO
cristin.unitcode194,66,25,0
cristin.unitnameInstitutt for kjemi
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode1


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