Studies towards the total syntheses of solandelactones: Stereoselective synthesis of the cyclopropane - lactone segment
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Solandelactones A-I, lactonized cyclopropyl oxylipins isolated from the hydroid Solanderia secunda
2. Isolation and structure of constanolactones A and B, new cyclopropyl hydroxy-eicosanoids from the temperate red alga constantinea simplex
3. Structure and stereochemistry of constanolactones A-G, lactonized cyclopropyl oxylipins from the red marine alga Constantinea simplex
4. Halicholactone and neohalicholactone, two novel fatty acid metabolites from the marine sponge kadota
5. The three-dimensional structure of neohalicholactone, an unusual fatty acid metabolite from the marine sponge halichondria okadai kadota
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1. Concise Formal Synthesis on Solandelactone E Based on a Regioselective Cyclopropanation;HETEROCYCLES;2023
2. Total Synthesis of Chlorinated Oxylipin Eiseniachloride B;Chemical and Pharmaceutical Bulletin;2021-06-01
3. Cyclopropyl Lactone-Containing Marine Oxylipins;Studies in Natural Products Chemistry;2018
4. Total Synthesis of Solandelactone I;Journal of Natural Products;2015-11-12
5. Total Synthesis of Solandelactones A and B;European Journal of Organic Chemistry;2015-07-30
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