Zaragozic acid: Unusual stereochemical dependence in anhydride formation of carbohydrate templates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Zaragozic acid A, a potent inhibitor of squalene synthase: initial chemistry and absolute stereochemistry
2. The zaragozic acids: Structure elucidation of a new class of squalene synthase inhibitors
3. Synthetic studies towards the squalestatins and zaragozic acids
4. The first synthesis of the novel 2,8-dioxabicyclo[3.2.1]octane ring system: a key feature of the squalestatins
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1. The Construction of Anhydro Monosaccharides;Asian Journal of Organic Chemistry;2016-10-25
2. The Chemistry of L ‐Sorbose;European Journal of Organic Chemistry;2011-03-22
3. Total Syntheses of Zaragozic Acids A and C by a Carbonyl Ylide Cycloaddition Strategy;Chemistry - A European Journal;2006-12-04
4. Total synthesis of zaragozic acid C by an aldol-based strategy;Tetrahedron;2005-11
5. Sugars as Chiral Starting Materials in Enantiospecific Synthesis;The Organic Chemistry of Sugars;2005-09-21
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