Chiral approach to total synthesis of phytotoxic and related nonenolides: (Z)-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon-4-eno-9-lactone, herbarumin-III and their C-9 epimers
Author:
Funder
CSIR-UGC
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Natural ten-membered lactones: sources, structural diversity, biological activity, and intriguing future;Natural Product Reports;2024
2. The Role of Total Synthesis in Structure Revision and Elucidation of Decanolides (Nonanolides);Progress in the Chemistry of Organic Natural Products 115;2021
3. A Chiron Approach to the Stereoselective Total Synthesis of Phomonol and Phytotoxic Nonenolides;European Journal of Organic Chemistry;2020-02-10
4. Stagonolides J and K and Stagochromene A, Two New Natural Substituted Nonenolides and a New Disubstituted Chromene-4,5-dione Isolated from Stagonospora cirsii S-47 Proposed for the Biocontrol of Sonchus arvensis;Journal of Agricultural and Food Chemistry;2019-10-31
5. Divergent total synthesis of aspinolides B, E and J;Tetrahedron;2019-07
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