Enantioselective Hydroxylation of Benzylic C(sp3)–H Bonds by an Artificial Iron Hydroxylase Based on the Biotin–Streptavidin Technology
Author:
Affiliation:
1. Department of Chemistry, University of Basel, BPR1096, Mattenstrasse 24a, CH-4058 Basel, Switzerland
2. Department of Chemistry and Biochemistry, Texas State University, 78666 Texas, United States
Funder
Schweizerischer Nationalfonds zur F?rderung der Wissenschaftlichen Forschung
H2020 Marie Sklodowska-Curie Actions
Universit?t Basel
H2020 European Research Council
European Molecular Biology Organization
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
http://pubs.acs.org/doi/pdf/10.1021/jacs.0c02788
Reference71 articles.
1. Undirected, Homogeneous C–H Bond Functionalization: Challenges and Opportunities
2. C–H activation
3. Chiral Diaryliodonium Phosphate Enables Light Driven Diastereoselective α-C(sp3)–H Acetalization
4. Evolution of C–H Bond Functionalization from Methane to Methodology
5. C–H bond activation enables the rapid construction and late-stage diversification of functional molecules
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