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|Type:||Artigo de periódico|
|Title:||Enantioselective benzylic microbial hydroxylation of indan and tetralin|
|Abstract:||A screening with 15 strains of bacteria and fungi targeted at the production of specific hydroxylated benzylic derivatives of indan 1 and tetralin 2 was carried out. Mortierella isabellina, Mortierella ramanniana and Beauveria bassiana were shown to mediate the respective conversions to 1-indanol (3) and 1-tetralol (4), the most satisfactory results being obtained with M. isabellina, which gave 78% conversion of I to (1R)-3 (64% yield, 86% ee) after a 2-day-incubation, and 52% conversion of 2 to (IR)-4 (38% yield, 92% ee) in a 4-day-incubation. Over-oxidation of alcohols 3 and 4 during the reactions resulted on the formation of 1-indanone and 2-tetralone, respectively. (c) 2007 Elsevier B.V. All rights reserved.|
|Editor:||Elsevier Science Bv|
|Citation:||Journal Of Molecular Catalysis B-enzymatic. Elsevier Science Bv, v. 46, n. 41730, n. 37, n. 42, 2007.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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