Absolute and Relative Configuration of Erythroskyrin
- 1 May 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Natural Products
- Vol. 51 (3) , 562-566
- https://doi.org/10.1021/np50057a018
Abstract
We have reisolated erythroskyrin [1] from Penicillium islandicum and have determined the relative stereochemistry of the compound through extensive 1H- and 13C-nmr studies. The absolute stereochemistry was determined by nmr studies of the O-methylmandelate esters.This publication has 4 references indexed in Scilit:
- CD additivity in trichothecene benzoates: application as a microanalytical method for trichothecene characterizationTetrahedron, 1986
- Tetronomycin, a novel polyether of unusual structure.The Journal of Antibiotics, 1982
- Metabolic Products of Fungi. XXIV. The Structure of Erythroskyrine, a Nitrogen-containing Coloring Matter of Penicillium islandicum SoppCHEMICAL & PHARMACEUTICAL BULLETIN, 1964
- Studies in the biochemistry of micro-organisms. 92. The colouring matters of Penicillium islandicum Sopp Part 4. Iridoskyrin, rubroskyrin and erythroskyrineBiochemical Journal, 1954