72142-97-3Relevant articles and documents
Microwave-accelerated solvent-free synthesis of thioketones, thiolactones, thioamides, thionoesters, and thioflavonoids
Varma, Rajender S.,Kumar, Dalip
, p. 697 - 700 (2008/02/11)
Formula presented An expeditious, solvent-free, and high yield conversion of ketones, flavones, isoflavones, lactones, amides, and esters to the corresponding thio analogues is described utilizing Lawesson's reagent in a process that circumvents the use of dry solvents and excess of the reagent.
PHOTOBIOLOGICAL PROPERTIES OF FUROTHIOCOUMARINS IN SACCHAROMYCES CEREVISIAE
Juettermann, R.,Averbeck, D.,Averbeck, S.,Bastian, G.,Royer, R.
, p. 3 - 13 (2007/10/02)
Nine furothiocoumarins corresponding to psoralen, 8-methylpsoralen, 3-carbethoxy-8-methylpsoralen, 8-methoxysporalen, pseudosporalen, angelicin, isopseudosporalen, allopsoralen and pseudoisosporalen were synthesized by treating furocoumarins with phosphorus pentasulfide. Photobiological studies on haploid yeast cells (Saccharomyces cerevisiae) revealed that the furocoumarins exert some photoactivity on cell survival and the induction of mitochondrial damage.In most cases, the furothiocoumarins were less active than their furocoumarinic counterparts and exhibited a preference for a monofunctional type of action.A certain photochemotherapeutic activity can be suggested.