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dc.contributor.authorNeeranuth Intakaewen_US
dc.contributor.authorPuracheth Rithchumponen_US
dc.contributor.authorChanatkran Promminen_US
dc.contributor.authorSaranphong Yimklanen_US
dc.contributor.authorNawee Kungwanen_US
dc.contributor.authorPraput Thavornyutikarnen_US
dc.contributor.authorPuttinan Meepowpanen_US
dc.description.abstract© 2019 The Royal Society of Chemistry. New alternative chiral derivatizing agents, β-keto-anthracene adducts (KAAs), were accomplished and the influence of aromatic moieties at the α-carbon position for elucidation of the absolute configuration of chiral secondary alcohols via NMR was studied. The α-benzoyl substituted KAAs strongly enhance the anisotropic effect which produced greater ΔδRS values than other conventional reagents. We propose a simplified model to describe the conformations and to assign the absolute configuration in several chiral alcohol samples.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleSynthesis and characterization of novel chiral derivatizing agents containing β-keto-anthracene adducts (KAAs) by <sup>1</sup>H-NMR: Aromatic influence and chiral alcohol absolute configuration determinationen_US
article.title.sourcetitleOrganic and Biomolecular Chemistryen_US
article.volume17en_US Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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