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Please use this identifier to cite or link to this item: https://doi.org/10.21256/zhaw-3684
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dc.contributor.authorMazenauer, Manuel R.-
dc.contributor.authorManov, Stole-
dc.contributor.authorGalati, Vanessa M.-
dc.contributor.authorKappeler, Philipp-
dc.contributor.authorStohner, Jürgen-
dc.date.accessioned2018-06-01T10:33:49Z-
dc.date.available2018-06-01T10:33:49Z-
dc.date.issued2017-
dc.identifier.issn2046-2069de_CH
dc.identifier.urihttps://digitalcollection.zhaw.ch/handle/11475/6407-
dc.description.abstractChiral halomethane is the smallest stable molecule with a single asymmetric C-atom and halogenated acetic acids often serve as precursors. We focus on a synthetic route to synthesise chiral halogenated acetic acids with F, Cl, Br, and H/D isotopic substitution at the α-C-atom starting from diethyl malonate. This reactant is easily available, cheap and allows the obtainment of target acids in a few reaction steps with great versatility. Among all of the possible fully halogenated acetic acids (more than one hundred, which are, in principle, accessible by this route), there are only a small number of chiral halogenated acetic acids, which have been synthesized following the devised synthetic route.de_CH
dc.language.isoende_CH
dc.publisherRoyal Society of Chemistryde_CH
dc.relation.ispartofRSC Advancesde_CH
dc.rightshttp://creativecommons.org/licenses/by/3.0/de_CH
dc.subject.ddc540: Chemiede_CH
dc.titleSynthetic routes for a variety of halogenated (chiral) acetic acids from diethyl malonatede_CH
dc.typeBeitrag in wissenschaftlicher Zeitschriftde_CH
dcterms.typeTextde_CH
zhaw.departementLife Sciences und Facility Managementde_CH
zhaw.organisationalunitInstitut für Chemie und Biotechnologie (ICBT)de_CH
dc.identifier.doi10.21256/zhaw-3684-
dc.identifier.doi10.1039/C7RA09727Ade_CH
zhaw.funding.euNode_CH
zhaw.issue87de_CH
zhaw.originated.zhawYesde_CH
zhaw.pages.end55440de_CH
zhaw.pages.start55434de_CH
zhaw.publication.statuspublishedVersionde_CH
zhaw.volume7de_CH
zhaw.publication.reviewPeer review (Publikation)de_CH
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Mazenauer, M. R., Manov, S., Galati, V. M., Kappeler, P., & Stohner, J. (2017). Synthetic routes for a variety of halogenated (chiral) acetic acids from diethyl malonate. RSC Advances, 7(87), 55434–55440. https://doi.org/10.21256/zhaw-3684
Mazenauer, M.R. et al. (2017) ‘Synthetic routes for a variety of halogenated (chiral) acetic acids from diethyl malonate’, RSC Advances, 7(87), pp. 55434–55440. Available at: https://doi.org/10.21256/zhaw-3684.
M. R. Mazenauer, S. Manov, V. M. Galati, P. Kappeler, and J. Stohner, “Synthetic routes for a variety of halogenated (chiral) acetic acids from diethyl malonate,” RSC Advances, vol. 7, no. 87, pp. 55434–55440, 2017, doi: 10.21256/zhaw-3684.
MAZENAUER, Manuel R., Stole MANOV, Vanessa M. GALATI, Philipp KAPPELER und Jürgen STOHNER, 2017. Synthetic routes for a variety of halogenated (chiral) acetic acids from diethyl malonate. RSC Advances. 2017. Bd. 7, Nr. 87, S. 55434–55440. DOI 10.21256/zhaw-3684
Mazenauer, Manuel R., Stole Manov, Vanessa M. Galati, Philipp Kappeler, and Jürgen Stohner. 2017. “Synthetic Routes for a Variety of Halogenated (Chiral) Acetic Acids from Diethyl Malonate.” RSC Advances 7 (87): 55434–40. https://doi.org/10.21256/zhaw-3684.
Mazenauer, Manuel R., et al. “Synthetic Routes for a Variety of Halogenated (Chiral) Acetic Acids from Diethyl Malonate.” RSC Advances, vol. 7, no. 87, 2017, pp. 55434–40, https://doi.org/10.21256/zhaw-3684.


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