171868-66-9Relevant articles and documents
Lipase AK-mediated synthesis of both antipodes of 2-phenyl- and 2-(1-naphthyl)cyclohexanols in enantiomerically pure form
She, Yi-Hsuan,Wu, Chen-Fan,Shia, Kak-Shan,Wu, Jen-Dar,Peddinti, Rama Krishna,Liu, Hsing-Jang
, p. 749 - 752 (2005)
Both (R,S)- and (S,R)-enantiomers of 2-phenylcyclohexanol and 2-(1-naphthyl)cyclohexanol were prepared in enantiomerically pure form and in excellent chemical yields by lipase AK (Pseudomonas fluorescens)-catalyzed kinetic acetylation of racemic alcohols
Preparation of Enantiomerically Pure trans- and cis-2-(1-Naphthyl)cyclohexan-1-ols
Takahashi, Michiyasu,Ogasawara, Kunio
, p. 1617 - 1620 (2007/10/02)
Lipase-mediated treatment of racemic trans-2-(1-naphthyl)cyclohexan-1-ol with vinyl acetate allows clear-cut enantiospecific kinetic acetylation to give (+)-(1R,2S)-acetate in excellent chemical and enantiomeric excesses leaving (+)-(1S,2R)-alcohol in an