4.7 Article

Regio- and enantioselective catalytic hydrophosphorylation of vinylarenes

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 347, Issue 5, Pages 667-672

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200404390

Keywords

asymmetric catalysis; hydrophosphorylation; palladium; P ligands; rhodium

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Regioselective and stereoselective hydrophosphorylation of vinylarenes 1 with pinacol H-phosphonate 2 can be achieved with transition metal catalysts. The use of rhodium catalysts such as the Wilkinson complex leads to the anti-Markovnikov adducts 3 as the only observable reaction products. In contrast, palladium catalysts give high selectivities for the Markovnikov adducts 4. In the presence of (R,S)-BINAPHOS as a chiral ligand, significant enantioselectivities have been obtained for the first time in hydrophosphorylation reactions.

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