Biocatalytic preparation of optically active 4-(N, N-dimethylamino) pyridines for application in chemical asymmetric catalysis
E Busto, V Gotor-Fernández, V Gotor
Index: Busto, Eduardo; Gotor-Fernandez, Vicente; Gotor, Vicente Tetrahedron Asymmetry, 2006 , vol. 17, # 6 p. 1007 - 1016
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Citation Number: 22
Abstract
4-Chloro-2-(1-hydroxybenzyl) pyridine and 4-chloro-2-(1-hydroxyalkyl) pyridines were obtained with moderate to excellent enantiomeric excesses and high isolated yields by bioreduction with Baker's yeast of the corresponding ketones. The resulting optically active alcohols were transformed into adequate DMAP derivatives, which have been applied in asymmetric catalytic processes as nucleophilic catalysts in the stereoselective chemical ...
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[Busto, Eduardo; Gotor-Fernandez, Vicente; Gotor, Vicente Tetrahedron Asymmetry, 2005 , vol. 16, # 20 p. 3427 - 3435]