Plausible reaction pathway for thiocyanation of arylboronic acids with TMSNCS
A mild copper-catalyzed aerobic oxidative thiocyanation of arylboronic acids with TMSNCS
Figure 1
From these results, a plausible reaction mechanism is proposed in Figure 1. It was assumed that LCu(I)Cl A was first exchanged with the in situ generated NCS-anion to form reactive LCu(I)SCN B, which could be oxidized by O2 to yield bis(µ-oxo)-dicopper (III) complex C. In this step, the existence of the diamine ligand TMEDA (L) was essential.
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