The copper(I)‐catalyzed (2+3) cycloaddition between azido (or azidomethylene) ferrocenes and enantiopure (P)‐14‐(p‐ethynylphenyl)‐5]‐tetrahydro‐helicenequinone afforded ferrocene–triazole–quinone triads, whereas diazido ferrocenes gave rise to the corresponding double triads. In reactions with 1,1′‐diazidoferrocene, the use of CuI/CH3CN or CuSO4/sodium ascorbate/THF conditions allowed the divergent formation of an open chain dimeric structure or a 1,4‐diaza‐4]‐ferrocenophane resulting from an intramolecular oxidative coupling of the two triazole units formed after the double cycloaddition process.
