4.8 Article

Iridium-N,P-Ligand-Catalyzed Enantioselective Hdyrogenation of Diphenylvinylphosphine Oxides and Vinylphosphonates

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 23, Pages 8285-8289

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja901437t

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Diphenylvinylphosphine oxides and di- and trisubstituted vinylphosphonates have been employed as substrates in iridium-catalyzed asymmetric hydrogenations. Complete conversions and excellent enantioselectivities (up to and above 99% ee) were observed for a range of substates with both aromatic and aliphatic groups at the prochiral carbon. We have also hydrogenated electron-deficient carboxyethylvinylphosphonates with excellent stereoselectivity (up to and above 99% ee). The hydrogenated products of both classes of substrates are synthetically useful intermediates.

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