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|Type:||Artigo de Periódico|
|Title:||Deracemization Of 1-phenylethanol Via Tandem Biocatalytic Oxidation And Reduction|
|Abstract:||(R)-1-Arylethanols and other secondary alcohols were prepared at high ee (>90%) by oxidative kinetic resolution using resting cells of the yeast Candida albicans CCT 0776. The deracemization process of 1-phenylethanol la catalyzed by the yeast was elucidated by studying each step separately. It was determined that the reaction occurred via cyclic deracemization, to give (R)-1a in 89% yield and with 98% ee. Finally, deracemization by stereoinversion of rac-1a was studied using a tandem process of C. albicans followed by Lactobacillus brevis CCT 3745. Inverting the sequence of these microorganisms produced an enantiomerically pure antipode. (C) 2016 Published by Elsevier Ltd.|
|Editor:||PERGAMON-ELSEVIER SCIENCE LTD|
|Citation:||Tetrahedron: Asymmetry. PERGAMON-ELSEVIER SCIENCE LTD, n. 27, n. 9-10, p. 404 - 409.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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