A convenient approach to the asymmetric Strecker reaction was established by synthesizing chiral, mono- and dinuclear, macrocyclic MnIII–salen complexes possessing achiral and chiral linkers (trigol, piperazine, and diethyl tartarate). This group of macrocyclic complexes has emerged as improved metal-based catalysts for the enantioselective Strecker reaction of aldimines, giving high enantioselectivity (up to 99 %) for a wide range of substrates. The macrocylic complex 6 a with trigol linker works very well with TMSCN (trimethylsilyl cyanide) as a source of cyanide, using 4-phenyl pyridine N-oxide (4-PPyNO) as a co-catalyst in toluene at −40 °C. However, the macrocyclic complex 6 b with diethyl tartarate as a linker affected excellent chiral induction for both aromatic and aliphatic imines with a safer cyanide source (ethyl cyanoformate) in toluene at −20 °C in the presence of N,N-diisopropylimine as a co-catalyst. Complexes 6 a and 6 b used in the present study were recoverable and recyclable (five times) with retention of their performance at gram level. The kinetic study with complex 6 a for the enantioselective Strecker reaction of N-benzyl benzylimine revealed a first-order dependence on catalyst, substrate, and TMSCN concentration. This protocol with catalyst 6 b was further extended for the synthesis of D-homophenyl alanine, an important analogue in factor Xa inhibitors.