A novel axially dissymmetric ligand with chiral 2,2,2-trifluoro-1-hydroxyethyl groups
β Scribed by Masaaki Omote; Akane Kominato; Michi Sugawara; Kazuyuki Sato; Akira Ando; Itsumaro Kumadaki
- Book ID
- 104261866
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 153 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Novel axially dissymmetric ligands (1) with two more chiral carbons were synthesized through homo-coupling of o-bromo-(R or S)-(2,2,2-trifluoro-l-acetoxyethyl)benzene. A high asymmetric induction was accomplished using 5 mol% of the Ti complex of this ligand for the reaction of benzaldehyde with Et2Zn giving 85% ee of 1-phenylpropanol in 97% isolation yield.
π SIMILAR VOLUMES
The asymmetric preparation and metallation of binaphthylcyclopentadiene 1 is described. The key step in this four step synthesis is an asymmetric nickel-catalyzed coupling reaction. Chiral cyclopentadienyl ligands are becoming recognized as potent chiral auxiliaries for asymmetric organometallic rea
Enantiomerically pure hydroxy thiol (S)-(+)-6, amino thiol (S)-(+)-12, and N,N-dimethylamino thiol (S)-(-)-16 have been synthesized from BINOL (S)-(-)-1 and the amino alcohol (S)-(-)-7, respectively, via the Newman-Kwart rearrangement