An efficient synthesis of the 1,6-dioxaspiro[4.4]nonan-2-one motif of the immunosuppressive triterpenoid Phainanoid F
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Phainanoids A–F, A New Class of Potent Immunosuppressive Triterpenoids with an Unprecedented Carbon Skeleton from Phyllanthus hainanensis
2. Synthetic Study of Phainanoids. Highly Diastereoselective Construction of the 4,5-Spirocycle via Palladium-Catalyzed Intramolecular Alkenylation
3. Phainanolide A, Highly Modified and Oxygenated Triterpenoid from Phyllanthus hainanensis
4. Pyrenolide D, a New Cytotoxic Fungal Metabolite fromPyrenophora teres
5. Cytotoxic Styryl-Lactones from the Leaves and Twigs of Polyalthia crassa
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1. Synthesis towards Phainanoid F: Photo‐induced 6π‐Electrocyclization for Constructing Contiguous All‐Carbon Quaternary Centers;Chemistry – An Asian Journal;2023-09-14
2. Stereodivergent Construction of [5,5]-Oxaspirolactones of Phainanoids;The Journal of Organic Chemistry;2023-03-08
3. Asymmetric Total Synthesis of (+)-Phainanoid A and Biological Evaluation of the Natural Product and Its Synthetic Analogues;Journal of the American Chemical Society;2023-02-17
4. Bidirectional Total Synthesis of Phainanoid A via Strategic Use of Ketones;Journal of the American Chemical Society;2021-11-12
5. Synthetic Study Toward the 4,5-Spirocycle Skeleton of Phainanoids;Acta Chimica Sinica;2020
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