“…This was also the case of the electron-poor aromatic ring, pyridine-2-carboxaldehyde (entry 8), which was reduced only to the corresponding alcohol. Interestingly, however, is the fact that nitrobenzaldehydes (o, m, p) were fully reduced to the corresponding methylanilines (entries 4,11,12) with yields up to 85 %, suggesting that the nitro group is reduced first to the corresponding amine and later it would occur the HDO of the aldehyde moiety. To confirm this idea, using p-nitrobenzaldehyde, the reaction was controlled at different reaction times.…”