Palladium(ii)-catalyzed asymmetric hydrophosphination of enones: efficient access to chiral tertiary phosphines
Chemical Communications2010Vol. 46(37), pp. 6950–6950
Citations Over TimeTop 10% of 2010 papers
Abstract
Chiral tertiary phosphines were synthesized by asymmetric hydrophosphination of aromatic enones catalyzed by an organopalladium complex with high yields and stereoselectivity. The procedure offers practical access to chiral tertiary phosphines.
Related Papers
- → Novel 1,4-Palladium Migration in Organopalladium Intermediates Derived from o-Iodobiaryls(2002)176 cited
- → Palladiumsalze and Palladium- Komplexe in der präparativen organischen Chemie(1970)45 cited
- → General Discussion of the Methods of Synthesis andIn Situ Generation of Organopalladium Compounds(2003)4 cited
- → Chemistry of Monoorganopalladium Complexes Relevant to Catalysis(2000)3 cited
- → Organopalladium Compounds Containing Pd(0) and Pd(II). General Discussion of the Methods of Synthesis and in situ Generation of Organopalladium Compounds(2003)