e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
Helvetica chimica acta
1, 3??Oxathiolan??Synthese: Spirocyclische 1, 3??Oxathiolane aus der Lewis??Säure??katalysierten Umsetzung von cyclischen Trithiocarbonaten und Oxiranen
(Scheme 3). respectively. The reactions proceed regioselectively yielding 2-alky1 (5, 10) and 3-phenyl derivatives (6, 11) as the main products. From the reaction of 4 and 2- phenyloxirane (2e) with TiCl,, 2-phenyl-l, 4, 6, 9-tetrathia-spiro [4, 4] nonane (7) is isolated as a minor product. The molecular structures of Sa, 6e, and 7 are established by X-ray crystallography.