posted on 2022-06-16, 17:41authored byChristopher Cremer, Frederic W. Patureau
Very few elements
in the periodic system can catalytically activate
O2, such as in the context of cross-dehydrogenative couplings.
The development of O2-activating catalysts is essential
to enable new and sustainable reactivity concepts to emerge, because
these catalysts also often feature specific activating interactions
with the target substrates. In this context, the unprecedented Te(II)/Te(III)
catalyzed dehydrogenative C3–C2 dimerization of indoles is
described herein. The fact that O2 can be directly utilized
as a terminal oxidant in this reaction, as well as the absence of
any background reactivity without the redox-active Te catalyst, constitute
very important milestones for the fields of cross-dehydrogenative
couplings and tellurium catalysis.