Novel enantiopure ferrocene-based aminophosphine and diphosphine ligands fo
r asymmetric catalysts have been developed. In all cases a highly flexible
synthetic approach allowed access to ligands with different ferrocenyl back
bones and with a variety of functional group patterns. Procedures for the s
ynthesis of six families of ligands with either a homo- or heteroannularly
bridged ferrocene, ferrocenylmethyl, biferrocene, biferroceno-azepine or fe
rrocenyl-aryl framework are described in detail.