Application of Two Direct C(sp3)–H Functionalizations for Total Synthesis of (+)-Lactacystin
Author:
Affiliation:
1. Graduate School of Pharmaceutical Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
Funder
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol503291s
Reference80 articles.
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3. Inhibition of Proteasome Activities and Subunit-Specific Amino-Terminal Threonine Modification by Lactacystin
4. 20S Proteasome and Its Inhibitors: Crystallographic Knowledge for Drug Development
5. Inhibitors for the Immuno- and Constitutive Proteasome: Current and Future Trends in Drug Development
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