The reactivity and stereoselectivity showed by a new strain of Candida tropicalis in the reduction of prochiral ketones have been compared with the ones previously attained in our laboratory using microorganisms from the Brazilian biodiversity. In this manner, Candida tropicalis has demonstrated its versatility as stereoselective agent in the bioreduction of a series of aromatic ketones. These prochiral compounds were converted into their corresponding optically alcohols with moderate to excellent stereopreference depending on the substrate structure. Among ketones tested, nitroacetophenones were enzymatically reduced to enantiopure (S)-alcohol with complete conversion. © 2010 Sociedade Brasileira de Química.
CITATION STYLE
Vieira, G. A. B., De Freitas Araujo, D. M., Lemos, T. L. G., De Mattos, M. C., Da Conceição F. De Oliveira, M., Melo, V. M. M., … Gotor, V. (2010). Candida tropicalis CE017: A new Brazilian enzymatic source for the bioreduction of aromatic prochiral ketones. Journal of the Brazilian Chemical Society, 21(8), 1509–1516. https://doi.org/10.1590/S0103-50532010000800015
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