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Hydrogenation and transfer hydrogenation of imines with cyclohexa‐1,4‐dienes, as well as with a representative Hantzsch ester dihydrogen surrogate, are reported. Both processes are catalyzed by tethered Ru−S complexes but differ in the activation mode of the dihydrogen source: cooperative activation of the H−H bond at the Ru−S bond leads to the corresponding Ru−H complex and protonation of the sulfur...
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