Studies on the Regioselective Nucleophilic Aromatic Substitution (S<sub>N</sub>Ar) Reaction of 2‑Substituted 3,5-Dichloropyrazines
2013-05-03T00:00:00Z (GMT) by
Differences in regioselectivity were observed during the S<sub>N</sub>Ar reaction of amines with unsymmetrical 3,5-dichloropyrazines. This study revealed that when the 2-position of the pyrazine was occupied with an electron-withdrawing group (EWG), nucleophilic attack occurred preferentially at the 5-position. When the 2-position was substituted with an electron-donating group (EDG), nucleophilic attack occurred preferentially at the 3-position. These results are reported along with a computational rationale for the experimental observations based on the Fukui index at the reacting centers.
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