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dc.contributor.author | Roke, Diedrik |
dc.contributor.author | Fañanás Mastral, Martín |
dc.contributor.author | Feringa, Ben L. |
dc.date.accessioned | 2018-07-06T12:43:17Z |
dc.date.available | 2018-07-06T12:43:17Z |
dc.date.issued | 2016-11-01 |
dc.identifier.citation | Roke, 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.uri | http://hdl.handle.net/10347/16978 |
dc.description.abstract | Polypropionate 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.sponsorship | Financial 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.iso | eng |
dc.publisher | Royal Society of Chemistry |
dc.rights | © The Royal Society of Chemistry 2016 |
dc.title | Iterative catalyst controlled diastereodivergent synthesis of polypropionates |
dc.type | journal article |
dc.identifier.doi | 10.1039/c6qo00199h |
dc.relation.publisherversion | https://doi.org/10.1039/C6QO00199H |
dc.type.hasVersion | AM |
dc.identifier.essn | 2052-4129 |
dc.rights.accessRights | open access |
dc.contributor.affiliation | Universidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares |
dc.contributor.affiliation | Universidade de Santiago de Compostela. Departamento de Química Orgánica |
dc.description.peerreviewed | SI |
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