Abstract:
:The combination of catalytic amounts of optically active dipyridylphosphine and CuF(2) along with hydride donor PhSiH(3) generated in situ a remarkably reactive catalyst system (substrate-to-ligand molar ratio up to 100,000) for the highly enantioselective hydrosilylation of a broad spectrum of aryl alkyl ketones (up to 97% enantiomeric excess) in normal atmosphere and at mild conditions (ambient temperature to -20 degrees C, compatible with traces of moisture) in the absence of base additives. Furthermore, a highly effective catalytic asymmetric hydrosilylation of unsymmetrical diarylketones using this catalyst system was also realized (up to 98% enantiomeric excess). The introduction of the dipyridylphosphine ligands in the air-accelerated and inexpensive metal-mediated asymmetric hydrosilylation of ketones makes the present system highly attractive and thus provides an excellent opportunity for practical applications.
journal_name
Proc Natl Acad Sci U S Aauthors
Wu J,Ji JX,Chan ASdoi
10.1073/pnas.0409043102keywords:
subject
Has Abstractpub_date
2005-03-08 00:00:00pages
3570-5issue
10eissn
0027-8424issn
1091-6490pii
0409043102journal_volume
102pub_type
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