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Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12493
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dc.contributor.authorSoponpong J.
dc.contributor.authorDolsophon K.
dc.contributor.authorThongpanchang C.
dc.contributor.authorLinden A.
dc.contributor.authorThongpanchang T.
dc.date.accessioned2021-04-05T03:03:43Z-
dc.date.available2021-04-05T03:03:43Z-
dc.date.issued2019
dc.identifier.issn404039
dc.identifier.other2-s2.0-85059805363
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/12493-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85059805363&doi=10.1016%2fj.tetlet.2019.01.013&partnerID=40&md5=0218c68347ee364cccd5d50634cd65d9
dc.description.abstractThe structure of a constrained bicyclic chiral derivatizing agent (CDA), 1,2,3,4-tetrahydro-1,4-epoxynaphthalene-1-carboxylic acid, THENA 1, was modified by replacing both exo-methylene protons with deuterium atoms. The modified CDA, THENA-d 2 2, could be used to assign the absolute configuration of chiral secondary alcohols with good reliability. Compared with THENA, the multiplicity of the methylene proton signals in the 1 H NMR spectra of THENA-d 2 derivatives is less complicated and the new CDA thus offers simpler NMR spectra for data interpretation. © 2019 Elsevier Ltd
dc.subject1,2,3,4 tetrahydro 1,4 epoxynaphthalene 1 carboxylic acid
dc.subjectcarboxylic acid derivative
dc.subjectreagent
dc.subjectunclassified drug
dc.subjectArticle
dc.subjectchiral chromatography
dc.subjectchirality
dc.subjectcrystal structure
dc.subjectderivatization
dc.subjectproton nuclear magnetic resonance
dc.subjectreaction analysis
dc.subjectsynthesis
dc.subjectX ray diffraction
dc.titleApplication of deuterated THENA for assigning the absolute configuration of chiral secondary alcohols
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationTetrahedron Letters. Vol 60, No.6 (2019), p.497-500
dc.identifier.doi10.1016/j.tetlet.2019.01.013
Appears in Collections:Scopus 1983-2021

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