166376-78-9Relevant articles and documents
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