Biocatalytic Asymmetric Michael Additions of Nitromethane to α,β-Unsaturated Aldehydes via Enzyme-bound Iminium Ion Intermediates
Author:
Affiliation:
1. Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands
Funder
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
H2020 Leadership in Enabling and Industrial Technologies
H2020 European Research Council
Publisher
American Chemical Society (ACS)
Subject
Catalysis,General Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acscatal.9b00780
Reference30 articles.
1. Tripeptides as Efficient Asymmetric Catalysts for 1,4-Addition Reactions of Aldehydes to Nitroolefins–A Rational Approach
2. Tripeptides of the Type H-D-Pro-Pro-Xaa-NH2as Catalysts for Asymmetric 1,4-Addition Reactions: Structural Requirements for High Catalytic Efficiency
3. Catalytic Asymmetric Michael Reactions of Acetaldehyde
4. Diphenylprolinol Silyl Ether as Catalyst of an Asymmetric, Catalytic, and Direct Michael Reaction of Nitroalkanes with α,β-Unsaturated Aldehydes
5. Diphenylprolinol Silyl Ethers as Efficient Organocatalysts for the Asymmetric Michael Reaction of Aldehydes and Nitroalkenes
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