Shi‐Wen Huang, Bo Wang, Zixing Shan, Dejie Zhao
Abstract
Some chiral oxazaborolidinones were prepared from L-α-amino acids reacting with borane and used as a new type of catalysts for asymmetric reduction of acetophenone with borane to afford R-(+)-1-phenyl ethanol with 23–76%ee in high yield.
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Some chiral oxazaborolidinones were prepared from L-α-amino acids reacting with borane and used as a new type of catalysts for asymmetric reduction of acetophenone with borane to afford R-(+)-1-phenyl ethanol with 23–76%ee in high yield.
Key concepts: Acetophenone, Chemistry, Borane, Catalysis, Yield (engineering), Ethanol, Organic chemistry, Amino acid