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. Author manuscript; available in PMC: 2012 Oct 10.
Published in final edited form as: Angew Chem Int Ed Engl. 2011 Sep 12;50(42):9943–9947. doi: 10.1002/anie.201104361

Table 2.

Coupling of Aryl Halides with Secondary Alcohols[a]

graphic file with name nihms-368824-t0006.jpg

graphic file with name nihms-368824-t0007.jpg
[a]

Reaction conditions: ArX (1 mmol), alcohol (2 mmol), Cs2CO3 (1.5 mmol), (allylPdCl)2 (0.5 – 2.5 mol %), L4 (1.5 – 6 mol %), toluene (1 mL), 90 °C, 21 h; isolated yields (average of two or more runs).

[b]

200 mg of 4Å molecular sieves was added.

[c]

in Bu3N.

[d]

cyclohexanol (1.5 mmol) was used.

[e]

In Et3N.

[f]

24 h.