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. Author manuscript; available in PMC: 2014 Sep 16.
Published in final edited form as: Angew Chem Int Ed Engl. 2013 Aug 9;52(38):10.1002/anie.201304188. doi: 10.1002/anie.201304188

Table 1.

Cyanation of aryl chlorides[[a],[b]]

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L1 97% (0.2% P1) L1 95% (0.4% P1) L1 90% (0.6% P1) L1 97% (0.3% P1)[c]
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L2 94% (0.8% P2) L2 84% (1.8% P2)[d] L2 90% (0.8% P2) L2 92% (0.7% P2)
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L2 91% (0.8% P2) L2 92% (0.5% P2) L2 85% (3% P2)
[a]

Reaction conditions: aryl chloride (1 mmol), K4[Fe(CN)6]•3H2O (0.5 equiv), precatalyst (× mol %), ligand (× mol %) KOAc (0.125 equiv), dioxane (2.5 mL), H2O (2.5 mL).

[b]

Isolated yields, average of 2 independent runs.

[c]

10 mmol scale: 96% yield.

[d]

70 °C, 12 h.