Hans Wynberg, B.L. Feringa
Abstract
In the reaction of diethylzinc with benzaldehyde to produce ethyl phenyl carbinol, an e.e. of 80–90% is obtained using 2% of a chiral amino alcohol having an e.e. of 10–20% as catalyst.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
In the reaction of diethylzinc with benzaldehyde to produce ethyl phenyl carbinol, an e.e. of 80–90% is obtained using 2% of a chiral amino alcohol having an e.e. of 10–20% as catalyst.
Key concepts: Diethylzinc, Benzaldehyde, Chemistry, Enantioselective synthesis, Catalysis, Alcohol, Organic chemistry