Abstract
We report the development of a method to parameterize and predict the performance of structurally flexible β-turn-containing peptide catalysts, using the atroposelective bromination of 3-arylquinazolin-4(3H)-ones as a case study. The multivariate correlations obtained for tetrapeptides of two β-turn types, type I′ pre-helical and type II′ β-hairpin, indicate that although one conformer may be associated with a more dominant contribution to the observed enantioselectivity, it is possible that multiple conformers contribute to a complex transition state ensemble.
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CITATION STYLE
Crawford, J. M., Stone, E. A., Metrano, A. J., Miller, S. J., & Sigman, M. S. (2018). Parameterization and Analysis of Peptide-Based Catalysts for the Atroposelective Bromination of 3-Arylquinazolin-4(3H)-ones. Journal of the American Chemical Society, 140(3), 868–871. https://doi.org/10.1021/jacs.7b11303
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