0000000001313783

AUTHOR

Maksim Ošeka

showing 3 related works from this author

Asymmetric Organocatalytic Wittig [2,3]-Rearrangement of Oxindoles

2016

A highly enantioselective organocatalytic [2,3]-rearrangement of oxindole derivatives is presented. The reaction was catalyzed by squaramide, and this provides access to 3-hydroxy 3-substituted oxindoles in high enantiomeric purities.

asymmetric organocatalytic wittigIndolesStereoisomerism010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysischemistry.chemical_compoundCombinatorial Chemistry TechniquesOrganic chemistryOxindolePhysical and Theoretical Chemistryta116Molecular Structure010405 organic chemistryOrganic ChemistrySquaramideEnantioselective synthesisStereoisomerismAmidesOxindoles0104 chemical scienceschemistryWittig reactionEnantiomerOrganic Letters
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CCDC 1447017: Experimental Crystal Structure Determination

2016

Related Article: Maksim Ošeka, Mariliis Kimm, Sandra Kaabel, Ivar Järving, Kari Rissanen, and Tõnis Kanger|2016|Org.Lett.|18|1358|doi:10.1021/acs.orglett.6b00291

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates3-(1-(4-chlorophenyl)prop-2-en-1-yl)-3-hydroxy-1-(4-methylbenzyl)-13-dihydro-2H-indol-2-one
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CCDC 1447018: Experimental Crystal Structure Determination

2016

Related Article: Maksim Ošeka, Mariliis Kimm, Sandra Kaabel, Ivar Järving, Kari Rissanen, and Tõnis Kanger|2016|Org.Lett.|18|1358|doi:10.1021/acs.orglett.6b00291

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters7-fluoro-3-hydroxy-1-(4-methylbenzyl)-3-(1-phenylprop-2-en-1-yl)-13-dihydro-2H-indol-2-oneExperimental 3D Coordinates
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