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dc.contributor.authorPrentice, Callum
dc.contributor.authorMorrisson, James
dc.contributor.authorSmith, Andrew D.
dc.contributor.authorZysman-Colman, Eli
dc.date.accessioned2020-10-01T10:30:03Z
dc.date.available2020-10-01T10:30:03Z
dc.date.issued2020-09-29
dc.identifier270419149
dc.identifier3c6fa368-fea8-4226-8ead-abc43e442f5f
dc.identifier000576635600001
dc.identifier85094965885
dc.identifier.citationPrentice , C , Morrisson , J , Smith , A D & Zysman-Colman , E 2020 , ' Recent developments in enantioselective photocatalysis ' , Beilstein Journal of Organic Chemistry , vol. 2020 , no. 16 , pp. 2363-2441 . https://doi.org/10.3762/bjoc.16.197en
dc.identifier.issn1860-5397
dc.identifier.otherORCID: /0000-0002-2104-7313/work/81405742
dc.identifier.otherORCID: /0000-0001-7183-6022/work/81405998
dc.identifier.urihttps://hdl.handle.net/10023/20712
dc.descriptionAuthors thank AstraZeneca for funding (C. P). A.D.S. thanks the Royal Society for a Wolfson Research Merit Award.en
dc.description.abstractEnantioselective photocatalysis has rapidly grown into a powerful tool for synthetic chemists. This review describes the various strategies for creating enantioenriched products through merging enantioselective catalysis and photocatalysis, with a focus on the most recent developments and a particular interest in the proposed mechanisms for each. With the aim of understanding the scope of each strategy, to help guide and inspire further innovation in this field.
dc.format.extent79
dc.format.extent8964245
dc.language.isoeng
dc.relation.ispartofBeilstein Journal of Organic Chemistryen
dc.subjectEnantioenrichmenten
dc.subjectEnantionselective catalysisen
dc.subjectEnantioselective photocatalysisen
dc.subjectPhotocatalysisen
dc.subjectPhotochemistryen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleRecent developments in enantioselective photocatalysisen
dc.typeJournal itemen
dc.contributor.sponsorThe Royal Societyen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.3762/bjoc.16.197
dc.description.statusPeer revieweden
dc.identifier.grantnumberWM140071en


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