Abstract
AbstractSuccessive treatment of the anhydride acid (I) with CH2N2 (II) and the amino compounds (III) (the L‐enantiomers are used) yields the cyclohexanes (IVa) (two diastereomers are isolated) and (IVb) (only the major diastereomer is isolated); initial binding experiments reveal these structures to be highly effective chiral solvating agents for racemic amines such as (+)‐ and (‐)‐ephedrine.
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