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dc.contributor.authorTorres, Paulo
dc.contributor.authorBalcells Fluvià, Mercè
dc.contributor.authorCanela i Garayoa, Ramon
dc.date.accessioned2022-03-04T08:49:59Z
dc.date.available2022-03-04T08:49:59Z
dc.date.issued2021
dc.identifier.issn2470-1343
dc.identifier.urihttp://hdl.handle.net/10459.1/73169
dc.description.abstractThe Diels–Alder reaction is a prototypical example of a thermally allowed [4 + 2] cycloaddition with good control over the regio- and stereochemical outcomes. Therefore, Diels–Alder reactions in which adjacent stereocenters are generated at the two ends of the newly formed single bonds imply two different possible stereochemical outcomes. In cases where the dienophile has a single electron-withdrawing substituent, the outcome can often be predicted by applying the known “endo rule”. Furthermore, the use of chiral eutectic solvents in asymmetric synthesis has become a novel tool to maintain sustainability in organic synthesis. In the present work, a set of recyclable and sustainable bio-based deep eutectic solvents (DESs) was designed using hydrogen bond acceptors (HBAs) with a chiral center. These compounds were used in their racemic and enantiomerically enriched forms to prepare DESs with lactic acid (LA), glycerol (Gly), and ethylene glycol, which act as hydrogen bond donors (HBDs) in the corresponding eutectic mixture. These DESs were used as solvents to study the reaction between cyclopentadiene and ethyl acrylate or butyl acrylate in typical [4 + 2] cycloadditions. The best yields and endo-selectivity were achieved using LA as the HBD in the eutectic mixtures. The results and adduct ratios obtained show that these DESs were able to improve both reaction yields and selectivity when compared to those observed in organic solvents or ionic liquids. Moreover, the reaction products (adducts) were easily recovered with diethyl ether from the reaction mixture, where they appeared as an upper layer.ca_ES
dc.description.sponsorshipThe authors are grateful to the DBA center for providing the research facilities and equipment. DBA is a certified agent TECNIO in the category of technology developers from the Government of Catalonia. The authors would like to thank the Catalan Government for the quality accreditation given to the Agricultural Biotechnology and Bioeconomy Unit (2017 SGR 828). This work has been partially funded by the Spanish government grant (PID2019-110735RB-C21-MINECO/ FEDER) and Catalan government grant (2017 SGR 828).ca_ES
dc.language.isoengca_ES
dc.publisherAmerican Chemical Societyca_ES
dc.relationMINECO/PN2017-2020/PID2019-110735RB-C21ca_ES
dc.relation.isformatofReproducció del document publicat a https://doi.org/10.1021/acsomega.1c00980ca_ES
dc.relation.ispartofACS Omega, 2021, vol. 6, núm. 30, p.19392-19399ca_ES
dc.rightscc-by-nc-nd (c) Torres, 2021ca_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAdductsca_ES
dc.subjectMixturesca_ES
dc.subjectSolventsca_ES
dc.subjectOrganic compoundsca_ES
dc.subjectNoncovalent interactionsca_ES
dc.subject.otherCompostos orgànicsca_ES
dc.subject.otherQuímicaca_ES
dc.titleEffect of novel deep eutectic solvents on the endo/exo ratio of diels–alder reactions at room temperatureca_ES
dc.typeinfo:eu-repo/semantics/articleca_ES
dc.identifier.idgrec031973
dc.type.versioninfo:eu-repo/semantics/publishedVersionca_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_ES
dc.identifier.doihttps://doi.org/10.1021/acsomega.1c00980


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cc-by-nc-nd (c) Torres, 2021
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