ChemInform Abstract: Modular Amino Acids and β-Amino Alcohol-Based Chiral Ligands for Enantioselective Addition of Diethylzinc to Aromatic Aldehydes.
✍ Scribed by Shaohua Gou; Zhongbin Ye; Guangjun Gou; Mingming Feng; Jing Chang
- Publisher
- John Wiley and Sons
- Year
- 2011
- Weight
- 29 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
## Abstract Enantioselective addition of diethylzinc to a series of aromatic aldehydes was developed using a modular amino acid amide chiral ligand (2__S__)‐3‐phenyl‐__N__‐((__R__)‐1‐phenyl‐ethyl)‐2‐(tosylamino)propanamide without using titanium complex. The catalytic system employing 10 mol% of 1g
## Abstract Among 9 ligands tested, the derivative AAA is found to be the most efficient one and the e.e.
## Abstract New amino acid‐based modular chiral ligands were readily synthesized and used to catalyze the asymmetric conjugate addition of Et~2~Zn to various cyclic enones in the presence of a variety of copper sources. Moderately high __ee__ of up to 72% were obtained using ligand (__S__)‐**1e** u