Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/75510
Title: Synthesis and application of methyl itaconate-anthracene adducts in configuration assignment of chiral secondary alcohols by<sup>1</sup>H NMR
Authors: Puracheth Rithchumpon
Neeranuth Intakaew
Nopawit Khamto
Saranpong Yimklan
Piyarat Nimmanpipug
Praput Thavornyutikarn
Puttinan Meepowpan
Authors: Puracheth Rithchumpon
Neeranuth Intakaew
Nopawit Khamto
Saranpong Yimklan
Piyarat Nimmanpipug
Praput Thavornyutikarn
Puttinan Meepowpan
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry
Issue Date: 7-Nov-2021
Abstract: Novel 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.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85118263149&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/75510
ISSN: 14770520
Appears in Collections:CMUL: Journal Articles

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