The Recurring Roles of Chlorine in Synthetic and Biological Studies of the Lissoclimides
Author:
Affiliation:
1. Department of Chemistry, UC Irvine, 1102 Natural Sciences II, Irvine, California 92697-2025, United States
2. Department of Pharmaceutical Sciences, UC Irvine, 101 Theory, Suite 101, Irvine, California 92697-3958, United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
General Medicine,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.0c00866
Reference57 articles.
1. Site-Selective Aliphatic C–H Chlorination Using N-Chloroamides Enables a Synthesis of Chlorolissoclimide
2. Synthesis facilitates an understanding of the structural basis for translation inhibition by the lissoclimides
3. Understanding the role of intermolecular interactions between lissoclimides and the eukaryotic ribosome
4. A Chlorine-Atom-Controlled Terminal-Epoxide-Initiated Bicyclization Cascade Enables a Synthesis of the Potent Cytotoxins Haterumaimides J and K
5. Structural basis for the inhibition of the eukaryotic ribosome
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1. Catalytic Chemo-, Regio-, Diastereo-, and Enantioselective Bromochlorination of Unsaturated Systems Enabled by Lewis Base-Controlled Chloride Release;Journal of the American Chemical Society;2022-07-12
2. Continuous Flow Organocatalytic Chlorination of Alkenes;European Journal of Organic Chemistry;2021-09-24
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