The RuCl2(η1-Ph2PCH2CH2OCH3)2(diamine) complexes 2L1–2L5 have been prepared in high yields from the reaction of equimolar amounts of RuCl2(η2-Ph2PCH2CH2OCH3)21 with various kinds of chelating diamines L1–L5 to form five-membered chelates with ruthenium. These novel ruthenium(II) complexes have been used as catalysts in the asymmetric hydrogenation of the prochiral ketone trans-4-phenyl-3-butene-2-one 3, using 2-propanol and different types of cocatalysts. Whereas complexes with achiral diamines afforded the racemic alcohols, complexes with chiral diamines (R,R or S,S) allowed the formation of the corresponding enantiomerically enriched secondary alcohol (S or R) with ee values of 45%. In order to obtain the secondary alcohol with ee of >99%, the kinetic resolution of enantiomerically enriched trans-4-phenyl-3-butene-2-ol 3 was performed in a consecutive approach using either the lipase-catalyzed enantioselective transesterification of the alcohol with isopropenyl acetate as the acyl donor in toluene or the enantioselective hydrolysis of the corresponding acetate in buffer. The determination of the enantiomeric excess (ee) of the resulting enantiomerically enriched secondary alcohols was performed by gas chromatography using heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-β-cyclodextrin as the chiral stationary phase.

العنوان

Tetrahedron: Asymmetry, Volume 14, Issue 8, 18 April 2003, Pages 1045–1053

الناشر

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بلد الناشر

فلسطين

نوع المنشور

Both (Printed and Online)

المجلد

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السنة

2003

الصفحات

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