Toward the stereoselective synthesis of zaragozic acid framework: A desilylation-aldol reaction approach
- 21 October 2021
- journal article
- research article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 85, 153493
- https://doi.org/10.1016/j.tetlet.2021.153493
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Squalestatin protects neurons and reduces the activation of cytoplasmic phospholipase A2 by Aβ1–42Neuropharmacology, 2007
- Squalestatin Cures Prion-infected Neurons and Protects Against Prion NeurotoxicityOnline Journal of Public Health Informatics, 2004
- Trichloroisocyanuric/TEMPO Oxidation of Alcohols under Mild Conditions: A Close InvestigationThe Journal of Organic Chemistry, 2003
- Studies toward the Synthesis of Pinolidoxin, a Phytotoxic Nonenolide from the Fungus Ascochyta pinodes. Determination of the Configuration at the C-7, C-8, and C-9 Chiral Centers and Stereoselective Synthesis of the C6−C18 FragmentThe Journal of Organic Chemistry, 2000
- Chemistry and Biology of the Zaragozic Acids (Squalestatins)Angewandte Chemie, 1996
- DISCOVERY, BIOSYNTHESIS, AND MECHANISM OF ACTION OF THE ZARAGOZIC ACIDS: Potent Inhibitors of Squalene SynthaseAnnual Review of Microbiology, 1995
- Synthesis of Zaragozic Acid A/Squalestatin S1Chemistry – A European Journal, 1995
- A straightforward preparation of both enantiomerically pure 2-O-benzyl-erythro-butanetetrolsTetrahedron: Asymmetry, 1995
- Total Syntheses of Zaragozic AcidAngewandte Chemie, 1995
- The chemistry of L-ascorbic and D-isoascorbic acids. 1. The preparation of chiral butanetriols and -tetrolsThe Journal of Organic Chemistry, 1988