Abstract
An organocatalyzed intramolecular carbonyl-ene reaction was developed to produce carbocyclic and heterocyclic 5- and 6-membered rings from a citronellal-derived trifluoroketone and a variety of aldehydes. A phosphoramide derivative was found to promote the cyclization of the trifluoroketone, whereas a less acidic phosphoric acid proved to be a superior catalyst for the aldehyde substrates.
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Dahlmann, H. A., McKinney, A. J., Santos, M. P., & Davis, L. O. (2016). Organocatalyzed intramolecular carbonyl-ene reactions. Molecules, 21(6). https://doi.org/10.3390/molecules21060713
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