Synthetic studies toward phorboxazole A. Stereoselective synthesis of the C3C19 and C20C32 subunits
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Phorboxazoles A and B: potent cytostatic macrolides from marine sponge Phorbas species
2. Absolute Configuration of Phorboxazoles A and B from the Marine Sponge Phorbas sp. 1. Macrolide and Hemiketal Rings
3. Developments in Marine Natural Products. Receptor-Specific Bioactive Compounds
4. Absolute configuration of phorboxazoles A and B from the marine sponge, Phorbas sp. 2. C43 and complete stereochemistry
5. Synthetic studies towards phorboxazole A. A convergent synthesis of the C31C46 polyene oxane-hemiacetal side chain
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1. Applications of the Dess-Martin Oxidation in Total Synthesis of Natural Products;Current Organic Synthesis;2021-03
2. Synthesis of a Linear Fragment Containing the C23-C26 Stereocenters of Phorboxazole: A Flexible Molecule with Defined Conformation;Letters in Organic Chemistry;2018-05-09
3. Synthesis of β-(2,2-diethoxyethyl)-substituted (allyl)tributylstannane and its application to asymmetric allylation;Russian Journal of Organic Chemistry;2016-02
4. Porifera (Sponges)-5;Encyclopedia of Marine Natural Products;2014-08-07
5. Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads;Nat. Prod. Rep.;2014
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