Catalytic Asymmetric Synthesis of Butenolides and Butyrolactones

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Molecularesgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánicagl
dc.contributor.authorMao, Bin
dc.contributor.authorFañanás-Mastral, Martín
dc.contributor.authorFeringa, Ben L.
dc.date.accessioned2018-07-06T13:04:08Z
dc.date.available2018-07-06T13:04:08Z
dc.date.issued2017-06-22
dc.description.abstractγ-Butenolides, γ-butyrolactones, and derivatives, especially in enantiomerically pure form, constitute the structural core of numerous natural products which display an impressive range of biological activities which are important for the development of novel physiological and therapeutic agents. Furthermore, optically active γ-butenolides and γ-butyrolactones serve also as a prominent class of chiral building blocks for the synthesis of diverse biological active compounds and complex molecules. Taking into account the varying biological activity profiles and wide-ranging structural diversity of the optically active γ-butenolide or γ-butyrolactone structure, the development of asymmetric synthetic strategies for assembling such challenging scaffolds has attracted major attention from synthetic chemists in the past decade. This review offers an overview of the different enantioselective synthesis of γ-butenolides and γ-butyrolactones which employ catalytic amounts of metal complexes or organocatalysts, with emphasis focused on the mechanistic issues that account for the observed stereocontrol of the representative reactions, as well as practical applications and synthetic potentials.gl
dc.description.peerreviewedSIgl
dc.description.sponsorshipWe gratefully acknowledge generous support from The Netherlands Organization for Scientific Research (NWO-CW, Top grant to B.L.F.), the Royal Netherlands Academy of Arts and Sciences (KNAW), the Ministry of Education, Culture and Science (Gravitation Programme 024.001.035), the European Research Council (Advanced Investigator Grant 694345 to B.L.F.), and the Spanish Ministry of Economy and Competitiveness (Ramón y Cajal contract to M.F.-M.). B.M. gratefully thanks the Chinese National Natural Science Foundation (21606200) and the start-up fund from Zhejiang University of Technology for financial supportgl
dc.identifier.citationBin Mao, Martín Fañanás-Mastral, and Ben L. Feringa Chemical Reviews 2017 117 (15), 10502-10566 DOI: 10.1021/acs.chemrev.7b00151
dc.identifier.doi10.1021/acs.chemrev.7b00151
dc.identifier.essn1520-6890
dc.identifier.issn0009-2665
dc.identifier.urihttp://hdl.handle.net/10347/16979
dc.language.isoenggl
dc.publisherAmerican Chemical Societygl
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/694345
dc.relation.publisherversionhttps://doi.org/10.1021/acs.chemrev.7b00151gl
dc.rights© 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License, which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposesgl
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleCatalytic Asymmetric Synthesis of Butenolides and Butyrolactonesgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublication9dca33cc-3c8d-4d1c-8644-76987c972089
relation.isAuthorOfPublication.latestForDiscovery9dca33cc-3c8d-4d1c-8644-76987c972089

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