In Clayden's Organic Chemistry (Second Edition) it is written that borane is useful in chemoselectively reducing the most nucleophilic carbonyl to its corresponding alcohol. It is later said that DIBAL reacts similarly and is useful in reducing esters to aldehydes, but that they will not proceed to the alcohol.
How are these differences in reactivity rationalised? I tried to draw analogies from the comparison of $\ce{LiAlH4}$ and $\ce{NaBH4}$ but since $\ce{LiAlH4}$ is the stronger reductant, I would have expected DIBAL to be the more reactive species!