Abstract
Quinazolin-4-one derivatives possessing an isotopic atropisomerism (isotopic N-C axial chirality) based on ortho-12CH3/13CH3 discrimination were prepared. The diastereomeric quinazolin-4-ones bearing an asymmetric carbon as well as an isotopic atropisomerism were clearly discriminated by 1H and 13C NMR spectra and revealed to possess high rotational stability and stereochemical purity.
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CITATION STYLE
APA
Senda, R., Watanabe, Y., Miwa, S., Sato, A., & Kitagawa, O. (2023). Synthesis of Isotopic Atropisomers Based on 12C/13C Discrimination. Journal of Organic Chemistry, 88(13), 9579–9583. https://doi.org/10.1021/acs.joc.3c01004
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