Abstract
While purifying new polysubstituted 5-nitrosopyrimidines, the unique separation of pairs of rotamers as chemical species, stabilized by a single intramolecular hydrogen bond and differing only in nitroso group orientation, was achieved. This interesting stereochemical phenomenon is compared to the well-known atropisomerism. © The Partner Organisations 2014.
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CITATION STYLE
Cechová, L., Procházková, E., Císarová, I., Dracínský, M., & Janeba, Z. (2014). Separation of planar rotamers through intramolecular hydrogen bonding in polysubstituted 5-nitrosopyrimidines. Chemical Communications, 50(94), 14892–14895. https://doi.org/10.1039/c4cc06978a
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