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Effect of chiral N-substituents with methyl or trifluoromethyl groups on the catalytic performance of mono- and bifunctional thioureas.

Abstract

We evaluated thiourea organocatalysts that incorporate a chiral group which includes a trifluoromethyl moiety and contrasted their performance with non-fluorinated analogs. The comparison between such systems allows the direct study of the NH acidity of a thiourea bonded to an aliphatic substituent. In principle, the -CF3 systems feature an enhanced hydrogen bond (HB) donor capacity that was undoubtedly beneficial in HB-catalysis applied to the Baylis-Hillman reaction. We found that the thiourea substituted on both nitrogens with this group accelerates this reaction like Schreiner’s thiourea. On the other hand, we observed a different behavior in reactions promoted by bifunctional catalysts (thiourea-primary amine). In the Michael addition of isobutyraldehyde to methyl benzylidenepyruvate, the –CF3 containing catalysts were better than the –CH3 systems whereas the conjugate addition to N-phenylmaleimide showed the opposite behavior. Theoretical calculations of the transition states indicated that the phenylethyl group in fluorinated and non-fluorinated compounds have different kinds of interactions with the electrophile. These contacts are responsible for a different arrangement of the electrophile and thereby the selectivity of the catalyst. Therefore, it cannot be generalized that in all cases the NH acidity correlates with the performance of the catalyst, particulary, with aliphatic substituents that unlike the aromatic ones presents groups that are outside the plane of the thiourea.

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Publication details

The article was received on 29 Aug 2019, accepted on 08 Nov 2019 and first published on 08 Nov 2019


Article type: Paper
DOI: 10.1039/C9OB01893J
Org. Biomol. Chem., 2019, Accepted Manuscript

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    Effect of chiral N-substituents with methyl or trifluoromethyl groups on the catalytic performance of mono- and bifunctional thioureas.

    J. Vazquez-Chavez, S. Luna-Morales, D. A. Cruz-Aguilar, H. Díaz-Salazar, W. E. Vallejo Narváez, R. S. Silva-Gutiérrez, S. H. Ortega, T. Rocha-Rinza and M. Hernández-Rodríguez, Org. Biomol. Chem., 2019, Accepted Manuscript , DOI: 10.1039/C9OB01893J

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