Abstract
Aromatic nitriles are key structural units in organic chemistry and thus highly attractive targets for C–H activation. Herein the development of an arene-limited, nondirected C–H cyanation based on the use of two complementary ligands is reported. The reaction enables the cyanation of arenes by C–H activation in the absence of directing groups and is thus complementary to established approaches.
Supplementary materials
Title
Chen et al cyanation SI
Description
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