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Enantioselective Diethylzinc Addition to Aromatic Aldehydes Catalyzed by Novel Ti(IV) Complex of Three-Dentate Chiral Sulfonamide Ligands
β Scribed by Dabiri, Minoo; Salehi, Peyman; Heydari, Seddigheh; Kozehgary, Gholamreza
- Book ID
- 127210000
- Publisher
- Taylor and Francis Group
- Year
- 2009
- Tongue
- English
- Weight
- 278 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0039-7911
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π SIMILAR VOLUMES
The enantioselective addition of diethylzinc to aldehydes was conveniently achieved by using a catalyst prepared in situ by mixing titanium tetraisopropoxide with Sor R-binaphthol. Optical yields as high as 95.6% were obtained, t~) 1997 Elsevier Science Ltd. All rights reserved.
Enantioselective addition of diethylzinc to a series of aromatic aldehydes is developed using new chiral C 2 -symmetric ligand (S)-2,2 0 -(1,1 0 -binaphthyl-2,2 0 -diylbis(oxy))bis(methylene)bis(4-nitrophenol) (S)-2b. The catalytic system employing 10 mol % of (S)-2b and 120 mol % of Ti(OiPr) 4 was