Synthesis of three new bifunctional glucose-thiourea organocatalysts and their application in asymmetric Michael addition

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Abstract

Three new glucose-based asymmetric bifunctional organocatalysts containing a 6-aminopyridyl or a 6-methylpyridyl or a cinchona unit were synthesized. Asymmetric Michael addition of pentane-2,4-dione to β-nitrostyrene was catalyzed successfully by these catalysts. In case of the cinchona based glucose-thiourea derivate the S enantiomer of the corresponding Michael adduct was formed with moderate enantiomeric excess in three different solvents.

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Nagy, S., Kozma, P., Kisszékelyi, P., Bezzegh, D., Huszthy, P., & Kupai, J. (2017). Synthesis of three new bifunctional glucose-thiourea organocatalysts and their application in asymmetric Michael addition. Studia Universitatis Babes-Bolyai Chemia, 62(1), 183–194. https://doi.org/10.24193/subbchem.2017.1.16

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