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dc.creatorBondžić, Bojan
dc.creatorUrushima, Tatsuya
dc.creatorIshikawa, Hayato
dc.creatorHayashi, Yujiro
dc.date.accessioned2023-11-06T06:55:10Z
dc.date.available2023-11-06T06:55:10Z
dc.date.issued2010
dc.identifier.issn1523-7060
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/6812
dc.description.abstractAsymmetric epoxidation of α-substituted acroleins with hydrogen peroxide has been catalyzed by diphenylprolinol diphenylmethylsilyl ether to afford α-substituted-β,β-unsubstituted-α,β-epoxy aldehyde with excellent enantioselectivity and the generation of a chiral quaternary carbon center. The method was applied to a short synthesis of (R)-methyl palmoxirate.sr
dc.language.isoensr
dc.publisherAmerican Chemical Society (ACS)sr
dc.rightsrestrictedAccesssr
dc.sourceOrganic Letterssr
dc.subjectepoxidationsr
dc.subjectAsymmetric epoxidationsr
dc.subject(R)-methyl palmoxiratesr
dc.titleAsymmetric Epoxidation of α-Substituted Acroleins Catalyzed by Diphenylprolinol Silyl Ethersr
dc.typearticlesr
dc.rights.licenseARRsr
dc.citation.volume12
dc.citation.issue23
dc.citation.spage5434
dc.citation.epage5437
dc.citation.rankaM21
dc.identifier.pmid21049980
dc.identifier.doi10.1021/ol102269s
dc.identifier.scopus2-s2.0-78650339798
dc.type.versionpublishedVersionsr


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