A unique effect of styrene additive on product selectivity was observed for RuH(2)(CO)(PPh(3))(3)-catalyzed C-H arylation of acetophenone derivatives bearing two ortho C-H bonds. Without styrene, the C-H arylation with arylboronates gives diarylation products as the major products throughout the reaction, but the use of styrene as an additive switches the product selectivity and leads to selective formation of monoarylation products.

A convenient method for the synthesis of tetraalkylanthracenes and -pentacenes by means of ruthenium-catalyzed regioselective C-H alkylation of the corresponding acenequinones was developed. Dialkyldiarylpentacene was also synthesized using chemoselective tandem C-H alkylation/C-O arylation of dimethoxypentacenequinone. It was suggested that a tetraalkylpentacene is stable under air in the dark and possesses an appropriate HOMO level as active material for p-type organic field-effect transistors (OFETs).

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Control of Product Selectivity by a Styrene Additive in Ruthenium-Catalyzed C-H Arylation. -The selectivity in the mono-and disubstitution of acetophenones with aryl boronates (I) is investigated. Without an additive, the process gives mainly diarylation products as the major products, whereas the use of styrene results in selective formation of monoarylation products. -(HIROSHIMA, S.; MATSUMURA, D.; KOCHI, T.; KAKIUCHI*, F.; Org. Lett. 12 (2010) 22, 5318-5321, http://dx.

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