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dc.contributor.authorRoke, Diedrik
dc.contributor.authorFañanás Mastral, Martín
dc.contributor.authorFeringa, Ben L.
dc.date.accessioned2018-07-06T12:43:17Z
dc.date.available2018-07-06T12:43:17Z
dc.date.issued2016-11-01
dc.identifier.citationRoke, D., Fañanás-Mastral, M., & Feringa, B. (2016). Iterative catalyst controlled diastereodivergent synthesis of polypropionates. Organic Chemistry Frontiers, 3(11), 1383-1391. doi: 10.1039/c6qo00199h
dc.identifier.urihttp://hdl.handle.net/10347/16978
dc.description.abstractPolypropionate fragments are synthesized using a combination of a copper-catalyzed asymmetric allylic alkylation, ruthenium-catalyzed cross-metathesis and iridium-catalyzed asymmetric allylic etherification. The use of an appropriate chiral ligand for each catalytic reaction allows access to 1,2-hydroxymethyl arrays with good to excellent control over the relative and absolute configuration of the different stereocenters
dc.description.sponsorshipFinancial support from The Netherlands Organization for Scientific Research (NWO-CW), the National Research School of Catalysis (NRSC-C) and the Ministry of Education, Culture and Science (Gravitation Program 024.001.035) is gratefully acknowledged
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.rights© The Royal Society of Chemistry 2016
dc.titleIterative catalyst controlled diastereodivergent synthesis of polypropionates
dc.typejournal article
dc.identifier.doi10.1039/c6qo00199h
dc.relation.publisherversionhttps://doi.org/10.1039/C6QO00199H
dc.type.hasVersionAM
dc.identifier.essn2052-4129
dc.rights.accessRightsopen access
dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánica
dc.description.peerreviewedSI


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