Total synthesis of zaragozic acid C by an aldol-based strategy
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference113 articles.
1. Zaragozic acid A, a potent inhibitor of squalene synthase: initial chemistry and absolute stereochemistry
2. The isolation and structure elucidation of zaragozic acid C, a novel potent squalene synthase inhibitor.
3. Zaragozic acids: a family of fungal metabolites that are picomolar competitive inhibitors of squalene synthase.
4. The zaragozic acids: Structure elucidation of a new class of squalene synthase inhibitors
5. Zaragozic Acids D and D2: Potent Inhibitors of Squalene Synthase and of Ras Farnesyl-Protein Transferase
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1. Total Synthesis of (−)-Piericone D;The Journal of Organic Chemistry;2024-05-31
2. Stereo‐Controlled Synthesis of Vicinal Tertiary Carbinols: Application in the Synthesis of a Diol Substructure of Zaragozic Acid, Pactamycin and Ryanodol;Chemistry – A European Journal;2023-08-14
3. Diastereoselective and Enantioselective Synthesis of α-p-Methoxyphenoxy-β-Lactones: Dependence on the Stereoelectronic Properties of the β-Hydroxy-α-p-Methoxyphenoxycarboxylic Acid Precursors;The Journal of Organic Chemistry;2022-07-21
4. Development of Synthetic Strategies for Densely Oxygenated Natural Products: Total Synthesis of Lactacystin and Zaragozic Acid C Using Photochemical C(sp3)-H Functionalization;YAKUGAKU ZASSHI;2019-05-01
5. Advances in the Asymmetric Synthesis of Bridged and Fused Bicyclic Acetals;European Journal of Organic Chemistry;2018-10-10
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