Studies toward the synthesis of salinosporamide A, a potent proteasome inhibitor
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Salinosporamide A: A Highly Cytotoxic Proteasome Inhibitor from a Novel Microbial Source, a Marine Bacterium of the New Genus Salinospora
2. New Cytotoxic Salinosporamides from the Marine Actinomycete Salinispora tropica
3. A beta-lactone related to lactacystin induces neurite outgrowth in a neuroblastoma cell line and inhibits cell cycle progression in an osteosarcoma cell line.
4. A New Magnesium-Catalyzed Doubly Diastereoselective anti-Aldol Reaction Leads to a Highly Efficient Process for the Total Synthesis of Lactacystin in Quantity
5. Syntheses and Biological Evaluation of (+)-Lactacystin and Analogs
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1. Pyroglutamic Acid and its Derivatives: The Privileged Precursors for the Asymmetric Synthesis of Bioactive Natural Products;Mini-Reviews in Organic Chemistry;2020-08-24
2. Reactions of 3-pyrrolin-2-ones;Advances in Heterocyclic Chemistry;2019
3. Synthesis of 3,4-Fused γ-Lactone-γ-Lactam Bicyclic Moieties as Multifunctional Synthons for Bioactive Molecules;Journal of Heterocyclic Chemistry;2015-06-02
4. Eubacteria - 1;Encyclopedia of Marine Natural Products;2014-08-07
5. (S)-4-Trimethylsilyl-3-butyn-2-ol as an auxiliary for stereocontrolled synthesis of salinosporamide analogs with modifications at positions C2 and C5;Bioorganic & Medicinal Chemistry Letters;2013-12
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