Title of article :
Stereoinversion of 1-arylethanols by Cyanidioschyzon merolae NEIS-1332
Author/Authors :
Utsukihara، نويسنده , , Takamitsu and Misumi، نويسنده , , Osami and Nakajima، نويسنده , , Koichi and Koshimura، نويسنده , , Masahiro and Kuniyoshi، نويسنده , , Masayuki and Kuroiwa، نويسنده , , Tsuneyoshi and Horiuchi، نويسنده , , C. Akira، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
5
From page :
19
To page :
23
Abstract :
The stereoinversion of ortho-, meta- and para-substituted fluoro, chloro, bromo and methyl 1-phenylethanols using red alga (Cyanidioschyzon merolae) was investigated. It was found that 1-(4′-chlorophenyl)ethanol (1f) gave the corresponding (S)-alcohols in high ee and high yield (95%, 91% ee). On the other hand, stereoinversion of 1-(3′-chlorophenyl)ethanol (1e) indicated moderate ee (1e, 54% ee). In the case of 1-(2′-chlorophenyl)ethanol (1d), the biotransformation did not proceed. Moreover, we discuss about stereoinversion of alkyl group for secondary alcohols (3a–3d) and cis-2-methylcyclohexanol.
Keywords :
Acetophenone derivatives , 2-Methylcyclohexanone , Cyanidioschyzon merolae NEIS-1332 , red algae , Stereoinversion
Journal title :
Journal of Molecular Catalysis B Enzymatic
Serial Year :
2008
Journal title :
Journal of Molecular Catalysis B Enzymatic
Record number :
1713313
Link To Document :
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