The core issue here is microscopic reversibility: if an (auto)catalyst helps make one chirality form faster from an achiral starting system, it will also accelerate the reverse reaction. Autocatalysis can get you a transient spike in one chirality, but it can't sustain homochirality alone.
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if you looked purely at thermodynamics over kinetics, you'd conclude that benzene (∆Hf>0) is unstable relative to elemental C/H!