Enantiospecific Syntheses of Hongoquercins A and B and Chromazonarol
- 17 February 2017
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2017 (7), 1143-1150
- https://doi.org/10.1002/ejoc.201601503
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Meroterpenoids produced by fungiNatural Product Reports, 2009
- Synthesis of Marine Natural Products with Antimalarial ActivityMini-Reviews in Medicinal Chemistry, 2008
- The anti-angiogenic 8-epipuupehedione behaves as a potential anti-leukaemic compound against HL-60 cellsJournal of Cellular and Molecular Medicine, 2008
- An Efficient Stereoselective Synthesis of Cytotoxic 8-EpipuupehedioneJournal of Natural Products, 2003
- Hongoquercins A and B, New Sesquiterpenoid Antibiotics: Isolation, Structure Elucidation, and Antibacterial Activity.The Journal of Antibiotics, 1998
- Hongoquercins, New Antibacterial Agents from the Fungus LL-23G227: Fermentation and Biological Activity.The Journal of Antibiotics, 1998
- Evaluation of Marine Sponge Metabolites for Cytotoxicity and Signal Transduction ActivityJournal of Natural Products, 1993
- Puupehenone, A Cytotoxic Metabolite from a Deep Water Marine Sponge, Stronglyophora hartmaniJournal of Natural Products, 1987
- ent-Chromazonarol, a chroman-sesquiterpenoid from the spongeDisidea pallescensCellular and Molecular Life Sciences, 1975
- Darstellung und Valenzisomerisierung von Cyclobutenen mit „seitlich”︁ ankondensierten RingenEuropean Journal of Inorganic Chemistry, 1968