Recent advances in enantioselective desymmetrizations of prochiral oxetanes

dc.contributor.authorSandvoß, Alexander
dc.contributor.authorWiest, Johannes M.
dc.date.accessioned2021-06-22T11:09:10Z
dc.date.available2021-06-22T11:09:10Z
dc.date.issued2021
dc.description.abstractStrain relief of oxetanes offers a plethora of opportunities for the synthesis of chiral alcohols and ethers. In this context, enantioselective desymmetrization has been identified as a powerful tool to construct molecular complexity and this has led to the development of elegant strategies on the basis of transition metal, Lewis acid, and Brønsted acid catalysis. This review highlights recent examples that harness the inherent reactivity of prochiral oxetanes and offers an outlook on the immense possibilities for synthetic application.en_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-6017
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/6026
dc.language.isoeng
dc.rightsCC-BY-4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleRecent advances in enantioselective desymmetrizations of prochiral oxetanesen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.pricePAR-Fee
jgu.journal.issue19
jgu.journal.titleChemistry - a European journal
jgu.journal.volume27
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.end5879
jgu.pages.start5871
jgu.publisher.doi10.1002/chem.202004923
jgu.publisher.issn1521-3765
jgu.publisher.nameWiley-VCH
jgu.publisher.placeWeinheim
jgu.publisher.urihttps://doi.org/10.1002/chem.202004923
jgu.publisher.year2021
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode540
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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