An approach to the synthesis of furanoheliangolides through Diels–Alder reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Some Transformations of Adducts of 3,6-Dimethoxy-4,5-methylenedioxy-1,2-didehydrobenzene and Furans. An Approach to the 5,8-Dimethoxy-6,7-methylenedioxynaphtho[2,3-c]furan-4,9-dione Ring System of Ventilone A
2. Derivatives of 7-oxabicyclo[2.2.1]heptane in nature and as useful synthetic intermediates
3. Synthesis of 1-Methyl-3-oxo-7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylic Acid Methyl Ester
4. A Novel Anionic Condensation, Fragmentation, and Elimination Reaction of Bicyclo[2.2.1]heptenone Ring Systems
5. Flavonoids and heliangolides from Lychnophora diamantinana
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2. Synthesis of the bicyclo[6.2.1]undecane ring system by a solvent-free Diels–Alder reaction;Tetrahedron Letters;2014-01
3. Biomimetic synthesis of diversifolin;Tetrahedron Letters;2013-02
4. IrCl3 or FeCl3-catalyzed convenient synthesis of 3-hydroxyphthalates;Tetrahedron Letters;2011-11
5. Selectivity in reduction of natural furanoheliangolides with Stryker's reagent;Organic & Biomolecular Chemistry;2011
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