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dc.contributor.authorPuracheth Rithchumponen_US
dc.contributor.authorNeeranuth Intakaewen_US
dc.contributor.authorNopawit Khamtoen_US
dc.contributor.authorSaranpong Yimklanen_US
dc.contributor.authorPiyarat Nimmanpipugen_US
dc.contributor.authorPraput Thavornyutikarnen_US
dc.contributor.authorPuttinan Meepowpanen_US
dc.date.accessioned2022-10-16T07:00:23Z-
dc.date.available2022-10-16T07:00:23Z-
dc.date.issued2021-11-07en_US
dc.identifier.issn14770520en_US
dc.identifier.other2-s2.0-85118263149en_US
dc.identifier.other10.1039/d1ob01387den_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85118263149&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/75510-
dc.description.abstractNovel chiral derivatising agents (CDAs) such as methyl itaconate-anthracene adducts (MIAs) were reported for the absolute configuration determination of chiral secondary alcohols by the1H NMR technique. These adducts were facilely prepared through well-known reactions, and furthermore, commercially available starting materials. According to these synthetic routes, the desired MIAs were afforded in 6 steps with 49% overall yield from dimethyl itaconate. Moreover, the represented MIAs provided significantly large differences of chemical shift values (ΔδSR). No racemisation from the tertiary characteristics of the adjacent alpha carbon was observed.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleSynthesis and application of methyl itaconate-anthracene adducts in configuration assignment of chiral secondary alcohols by<sup>1</sup>H NMRen_US
dc.typeJournalen_US
article.title.sourcetitleOrganic and Biomolecular Chemistryen_US
article.volume19en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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