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2 changes: 1 addition & 1 deletion README.md
Original file line number Diff line number Diff line change
Expand Up @@ -91,7 +91,7 @@ blogposts with a decent writeup on the subject can be found [here][depth_first].
Despite how simple it seems at a glance, here be dragons lurking in the details.
The main problem is that in order to determine whether an edge is aromatic,
you need to generate *all* simple cycles. To illustrate why this is a problem,
let's look at buckminsterfullerene: it contains a staggering *15,024,073*
let's look at buckminsterfullerene: it contains a staggering *374,237,206*
cycles! It's really not feasible to investigate all of those separately.

Therefor we approximate the aromaticity for ring systems that are too large. By
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