Synthesis of lupinacidins A and B via sequential cycloaddition–double elimination
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Antitumor anthraquinones from an endophytic actinomycete Micromonospora lupini sp. nov.
2. Cycloadditions of o-quinone dimethides with p-quinol derivatives: regiocontrolled formation of anthracyclic ring systems
3. The colleflaccinosides, two chiral bianthraquinone glycosides with antitumor activity from the lichen Collema flaccidum collected in Israel and Russia
4. A bianthraquinone and 4′-O-methyl-ent-gallocatechin fromCassia trachypus
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1. Micromonospora: A Prolific Source of Bioactive Secondary Metabolites with Therapeutic Potential;Journal of Medicinal Chemistry;2022-06-29
2. Secondary Metabolites of Endophytic Actinomycetes: Isolation, Synthesis, Biosynthesis, and Biological Activities;Progress in the Chemistry of Organic Natural Products 108;2019
3. Synthesis of 1,3-Cycloalkadienes from Cycloalkenes: Unprecedented Reactivity of Oxoammonium Salts;Angewandte Chemie International Edition;2016-10-06
4. Synthesis of 1,3-Cycloalkadienes from Cycloalkenes: Unprecedented Reactivity of Oxoammonium Salts;Angewandte Chemie;2016-10-06
5. Lupinacidin C, an Inhibitor of Tumor Cell Invasion from Micromonospora lupini;Journal of Natural Products;2011-01-12
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