Abstract
Various aplysinopsin and β-carboline thiohydantoin analogues were prepared starting from ethyl 3-formyl-1H-indole-2-carboxylate by condensation with the active methylene group of 2-thiohydantoin, rhodanine, or thiobarbituric acid derivatives. © 2006 Verlag der Zeitschrift für Naturforschung.
Author supplied keywords
Cite
CITATION STYLE
Jakše, R., Bevk, D., Golobič, A., Svete, J., & Stanovnik, B. (2006). Synthesis and transformations of ethyl 3-formyl-1H-indole-2-carboxylate. Preparation of aplysinopsin and β-carboline thiohydantoin analogues. In Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences (Vol. 61, pp. 413–419). Verlag der Zeitschrift fur Naturforschung. https://doi.org/10.1515/znb-2006-0407
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
