Neomangicols: Structures and Absolute Stereochemistries of Unprecedented Halogenated Sesterterpenes from a Marine Fungus of the Genus Fusarium
- 22 October 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (23) , 8346-8354
- https://doi.org/10.1021/jo981226b
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Structure and Absolute Stereochemistry of Fusaproliferin, a Toxic Metabolite from Fusarium proliferatumJournal of Natural Products, 1996
- Penochalasins, a novel class of cytotoxic cytochalasans from a Penicillium species separated from a marine alga: structure determination and solution conformationJournal of the Chemical Society, Perkin Transactions 1, 1996
- Cytotoxic metabolites from a fungal adherent of a marine algaPhytochemistry, 1995
- Stachybotrins A and B: novel bioactive metabolites from a brackish water isolate of the fungus Stachybotrys spThe Journal of Organic Chemistry, 1992
- Variecolin, a sesterterpenoid of novel skeleton from Aspergillus variecolor MF138The Journal of Organic Chemistry, 1991
- Auranticins A and B: Two New Depsidones from a Mangrove Isolate of the Fungus Preussia aurantiacaJournal of Natural Products, 1991
- Norsesterterpenes from the North Adriatic Sponge Ircinia orosJournal of Natural Products, 1990
- Macromodel—an integrated software system for modeling organic and bioorganic molecules using molecular mechanicsJournal of Computational Chemistry, 1990
- An internal-coordinate Monte Carlo method for searching conformational spaceJournal of the American Chemical Society, 1989
- Reverse Phase Flash Chromatography: A Method for the Rapid Partitioning of Natural Product ExtractsJournal of Natural Products, 1987