Abstract
Enantioselective addition of diethylzinc to a series of aromatic aldehydes is developed using new chiral C2-symmetric ligand (S)-2,2′-(1,1′-binaphthyl-2,2′-diylbis(oxy))bis(methyl ene)bis(4-nitrophenol) (S)-2b. The catalytic system employing 10 mol % of (S)-2b and 120 mol % of Ti(OiPr)4 was found to promote the addition of diethylzinc to a wide range of aromatic aldehydes with electron-donating and electron-withdrawing substituents, giving up to 89% ee and up to 95% yield of the corresponding secondary alcohol under mild conditions.
Original language | English |
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Pages (from-to) | 281-283 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 50 |
Issue number | 3 |
DOIs | |
Publication status | Published - Jan 21 2009 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
Keywords
- Aldehyde
- Alkylation
- BINOL
- Chiral C-symmetric ligand
- Chiral core
- Diethylzinc
- Secondary alcohol
- Ti(OiPr)