Cyclocholates are efficiently and rapidly synthesised from suitable monomers by transesterification under thermodynamic, equilibrating conditions using a potassium methoxidexrown ether complex.

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A remarkably narrow product distribution is observed in the thermodynamic cyclization of modified Cinchona alkaloids to yield predominantly the trimer 1 (X = H, OMe); this is a representative of a new class of macrocycle. The reaction was proved to be reversible by resubmitting the cinchonidine (X = H) and quinine (X = OMe) to the reaction conditions: a statistical mixture of all four possible trimers was obtained.

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