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. Author manuscript; available in PMC: 2016 Jun 3.
Published in final edited form as: J Am Chem Soc. 2015 May 20;137(21):6742–6745. doi: 10.1021/jacs.5b03091

Table 1.

Scope of Enantioselective C–H Silylationa

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a

Isolated yields for reactions conducted on a 1.0 mmol scale following purification by silica gel chromatography. The ee values were determined by chiral HPLC analysis. The absolute configuration was assigned by analogy (see SI for details).

b

5.0 mmol scale.

c

The ee values were determined after iodination.

d

The reaction was conducted at 80 °C.

e

0.1 mol % [Ir(cod)OMe]2 was used for the first step.

f

The corresponding diarylmethanol was used as a substrate.

g

The ee value was determined after Tamao–Fleming oxidation.

h

The reaction was conducted at room temperature.