| Literature DB >> 30730598 |
Luca Dell'Amico1, Franca Zanardi2.
Abstract
Touched for the very first time! It is herein highlighted how acetaldehyde silyl enol ethers undergo enantioselective Mukaiyama aldol reaction with aliphatic and aromatic aldehydes. The chemistry relies on the use of the highly efficient and substrate-selective imidodiphosphorimidate catalyst, which displays some of the features of enzymatic catalysis.Entities:
Keywords: Mukaiyama aldol reaction; acetaldehyde; asymmetric synthesis; enzyme-like catalysis; organocatalysis
Year: 2019 PMID: 30730598 DOI: 10.1002/anie.201812964
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336