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Highly enantioselective catalytic phenylation of ketones with a constrained geometry titanium catalyst.

Organic letters (2003-09-26)
Celina García, Patrick J Walsh
RESUMEN

[reaction: see text] The catalytic asymmetric addition of phenyl groups from diphenylzinc to ketones is reported. The catalyst, generated from a dihydroxy bis(sulfonamide) ligand and titanium tetraisopropoxide, gives good to excellent enantioselectivities with a range of substrates.

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Sigma-Aldrich
3′-Chloropropiophenone, 98%