a. For the cis-substituted cyclohexanediamine structure, you can introduce the desired substituents selectively on the same face of the molecule. This can be achieved through a variety of reactions, such as reductive amination, acylation, or reactivity differences of functional groups. b. Use protecting groups, if necessary, to control the regioselectivity and avoid unwanted side reactions. For example, you can protect one amino group temporarily with a protecting group like a Boc (tert-butyloxycarbonyl) group.
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methyl 4-(hydroxy(2-oxocyclohexyl)methyl)benzoate
