Chiral thiolate-protected gold clusters of atomic precision have gained increasing interest in recent years due to their potential use in catalysis, sensing or bioapplications. While the protection of gold clusters with chiral ligands is a rather trivial task, it was found that the clusters can bear intrinsically chiral features, most obvious in the arrangement of the protecting ligands on the surface of the cluster. Recent efforts showed the separation of the enantiomers of such intrinsically chiral gold clusters. This technique can be used for the prediction of chirality in structurally unknown clusters. Activation barriers for the racemization of Au38(SR)24 were determined. As this involves a huge rearrangement of the ligands, the flexibility of the gold-thiolate interface is demonstrated. Furthermore, the ligand exchange reactions between intrinsically chiral clusters and bidentate chiral thiols were studied. A limited, regioselective exchange was found. Most importantly, the reaction is diastereoselective and allows tailoring of gold clusters that are protected with a defined layer of ligands.