Absolute stereochemistry of amphidinolide C: synthesis of C-1–C-10 and C-17–C-29 segments
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Amphidinolide W, a New 12-Membered Macrolide from Dinoflagellate Amphidinium sp.
2. Amphidinolide C: the first twenty-five membered macrocyclic lactone with potent antineoplastic activity from the cultured dinoflagellate Amphidinium sp
3. Bioactive metabolites of symbiotic marine microorganisms
4. Studies on the Stereochemistry of Amphidinolides: Synthesis of a Diastereomer of the C-1-C-9 Fragment of Amphidinolide C.
5. Absolute Stereochemistry of Amphidinolide C
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1. Advances Toward Amphidinolides C, F and U: Isolations, Synthetic Studies and Total Syntheses;Chemistry – A European Journal;2024-03-11
2. Synthetic Studies on Amphidinolide F: Exploration of Macrocycle Construction by Intramolecular Stille Coupling;Organic Letters;2022-10-12
3. Convergent Synthesis of the C1–C29 Framework of Amphidinolide F;The Journal of Organic Chemistry;2022-06-08
4. Amphidinolides F and C2: An Odyssey in Total Synthesis;The Journal of Organic Chemistry;2022-01-07
5. Studies toward the Synthesis of Amphidinolide C1: Stereoselective Construction of the C(1)–C(15) Segment;Organic Letters;2020-11-12
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