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- W238486595 abstract "During the development of hybrid chemopreventive agents containing chalcone framework and 3H-1,2dithiole-3-thione moiety an unexpected product was observed. When ADT-OH (Table 1) was subjected to classical alkylation conditions 1 , working in an excess of KI and K2CO3, we have obtained the resulting product of the electrophile character of the thiocarbonyl moiety on the 3-position of the 1,2dithiole, instead of the expected nucleophilic-reaction product. The aim of this work was rationalized this observed reactivity from an experimental and theoretical point of view." @default.
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- W238486595 date "2013-12-01" @default.
- W238486595 modified "2023-10-03" @default.
- W238486595 title "3H-1,2-dithiole-3-thione to (E)-3-[1-(alkylthio)alkylidene]-3H-1,2- dithiole transformation: theoretical and experimental studies" @default.
- W238486595 doi "https://doi.org/10.5151/chempro-15bmos-bmos2013_20139111275" @default.
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