Volume 27, Issue 11
Preparative Organic Chemistry
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ChemInform Abstract: Catalytic Asymmetric Hydrosilylation of Ketones with New Chiral Ferrocenylphosphine-Imine Ligands.

T. HAYASHI

T. HAYASHI

Dep. Chem., Fac. Sci., Kyoto Univ., Sakyo, Kyoto 606-01, Japan

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C. HAYASHI

C. HAYASHI

Dep. Chem., Fac. Sci., Kyoto Univ., Sakyo, Kyoto 606-01, Japan

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Y. UOZUMI

Y. UOZUMI

Dep. Chem., Fac. Sci., Kyoto Univ., Sakyo, Kyoto 606-01, Japan

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First published: March 12, 1996

Abstract

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ChemInform Abstract

The new chiral ferrocenylphosphine-imine ligands (IV) synthesized are found to be very effective for Rh-catalyzed asym. hydrosilylation of prochiral ketones with diphenylsilane to give optically active alcohols such as (VI) of up to 90% e.e. A slightly higher enantioselectivity is observed in reactions with the ligands (IVb) and (IVc) which are derived from aldehydes containing electron-withdrawing groups on the phenyl ring.

chemical structure image

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