Issue 15, 1997

Building thermodynamic combinatorial libraries of quinine macrocycles

Abstract

Thermodynamically-controlled transesterification of a predisposed cinchonidine building block with a more flexible extended quinine monomer leads to a combinatorial mixture of 11 macrocyclic receptors which is analysed by electrospray mass spectrometry; similar results with alkaloid–cholate mixtures demonstrate the generality of the approach.

Article information

Article type
Paper

Chem. Commun., 1997, 1407-1408

Building thermodynamic combinatorial libraries of quinine macrocycles

S. J. Rowan and J. K. M. Sanders, Chem. Commun., 1997, 1407 DOI: 10.1039/A703291I

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