Vis enkel innførsel

dc.contributor.authorVaitla, Janakiram
dc.contributor.authorGuttormsen, Yngve
dc.contributor.authorMannisto, Jere K.
dc.contributor.authorNova, Ainara
dc.contributor.authorRepo, Timo
dc.contributor.authorBayer, Annette
dc.contributor.authorHopmann, Kathrin Helen
dc.date.accessioned2018-09-10T12:10:18Z
dc.date.available2018-09-10T12:10:18Z
dc.date.issued2017-09-09
dc.description.abstractCO<sub>2</sub> is a promising and sustainable carbon feedstock for organic synthesis. New catalytic protocols for efficient incorporation of CO<sub>2</sub>into organic molecules are continuously being reported. However, little progress has been made in the enantioselective conversion of CO<sub>2</sub>to form enantioenriched molecules. In order to allow CO<sub>2</sub>to become a versatile carbon source in academia and in the fine chemical and pharmaceutical industries, the development of enantioselective approaches is essential. Here we discuss general strategies for CO<sub>2</sub>activation and for generation of enantioenriched molecules, alongside selected examples of reactions involving asymmetric incorporation of CO<sub>2</sub>. The main product classes considered are carboxylic acids and derivatives (C–CO<sub>2</sub>bonds) and carbonates, carbamates, and polycarbonates (C–OCO bonds). Similarities to asymmetric hydrogenation are discussed, and some strategies for developing novel enantioselective CO<sub>2</sub>reactions are outlined.en_US
dc.description.sponsorshipTromsø Research Foundation Magnus Ehrnrooth Foundationen_US
dc.descriptionThis document is the Accepted Manuscript version of a Published Work that appeared in final form in <i>ACS Catalysis</i>, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see <a href=https://doi.org/10.1021/acscatal.7b02306> https://doi.org/10.1021/acscatal.7b02306</a>.en_US
dc.identifier.citationVaitla, J., Guttormsen, Y., Mannisto, J.K., Nova, A., Repo, T., Bayer, A. & Hopmann, K.H. (2017). Enantioselective incorporation of CO2: status and potential. ACS Catalysis, 7(10), 7231-7244. https://doi.org/10.1021/acscatal.7b02306en_US
dc.identifier.cristinIDFRIDAID 1495918
dc.identifier.doi10.1021/acscatal.7b02306
dc.identifier.issn2155-5435
dc.identifier.urihttps://hdl.handle.net/10037/13741
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.journalACS Catalysis
dc.relation.projectIDinfo:eu-repo/grantAgreement/RCN/FRINATEK/231706/Norway/"Eeny, meeny, miny, moe": Selectivity-determining factors in asymmetric catalysis//en_US
dc.relation.projectIDinfo:eu-repo/grantAgreement/RCN/SFF/179568/Norway/Centre for Theoretical and Computational Chemistry/CTCC/en_US
dc.relation.projectIDinfo:eu-repo/grantAgreement/RCN/FRINATEK/250044/Norway/Rational catalyst design for transforming CO2 into industrially attractive products: Formic acid, polycarbonates and polyurethanes//en_US
dc.relation.urihttp://pubs.acs.org/articlesonrequest/AOR-j3TZbtYF3PxdiITGtc5Z
dc.rights.accessRightsopenAccessen_US
dc.subjectVDP::Matematikk og Naturvitenskap: 400::Kjemi: 440en_US
dc.subjectVDP::Mathematics and natural science: 400::Chemistry: 440en_US
dc.subjectasymmetric synthesisen_US
dc.subjectcarbamateen_US
dc.subjectcarbonateen_US
dc.subjectcarboxylic aciden_US
dc.subjectcatalysisen_US
dc.subjectCO2en_US
dc.subjectenantioselectivityen_US
dc.titleEnantioselective incorporation of CO2: status and potentialen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


Tilhørende fil(er)

Thumbnail

Denne innførselen finnes i følgende samling(er)

Vis enkel innførsel