125992-59-8Relevant academic research and scientific papers
Enzymic Preparation of Enantiomerically Pure Cyclohexanols: Ester Synthesis by Irreversible Acyl Transfer
Laumen, Kurt,Seemayer, Robert,Schneider, Manfred P.
, p. 49 - 51 (1990)
Enantiomerically pure cyclohexanols are prepared enzymically via irreversible acyl transfer; they are valuable substitutes for 8-phenylmenthols and are potentially useful as chiral auxiliaries.
Preparation and Enantiomer Recognition Behaviour of Azophenolic Crown Ethers containing cis-Cyclohexane-1,2-diol as a Chiral Centre
Naemura, Koichiro,Takeuchi, Sachiko,Hirose, Keiji,Tobe, Yoshito,Kaneda, Takahiro,Sakata, Yoshiteru
, p. 213 - 220 (2007/10/02)
Both enentiomers of the azophenolic crown ether 1 incorporating the cis-cyclohexane-1,2-diol residue as the chiral centre have been prepared in enantiomerically pure forms and the chiral recognition behaviour towards 2-aminoethanols and ethylamines has be
