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Synthesis, Chiral Separation, Barrier to Rotation and Absolute Configuration of N-(O- Functionalized-Aryl)-4-Alkyl-Thiazolin-2-One and Thiazoline-2-Thione Atropisomers
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2005
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-4-Alkyl-thiazolin-2-one AtropisomersThiazoline-2-thione AnaloguesAbsolute ConfigurationO- Functionalized-arylEngineeringHeterocyclicNatural SciencesDiversity-oriented SynthesisOrganic ChemistryStereoselective SynthesisChemistryHeterocycle ChemistryPharmacologyAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringChiral Separation
The synthesis of N-(o-aryl)-4-alkyl-thiazolin-2-one atropisomers bearing hydroxy-, methoxy-, amino- or isothiocyanato- groups as ortho-substituent are described from their thiazoline-2-thione analogues. The enantiomers were obtained optically pure by semi-preparative chiral HPLC, their optical properties and absolute configurations were established. The barriers to rotation were determined and are discussed according to the nature of the substituents. Keywords: heterocyclic atropisomer, barrier to rotation, absolute configuration