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- W4387298035 abstract "The direction of the reaction between substituted perfluorobenzenes and thioacetic acid depends on the location of the substituents in perfluoroaromatic ring. Hexafluorobenzene reacts at positions 1 and 4, perfluoro-m-xylene reacts at positions 4 and 6, while perfluoroindane reacts at positions 5 and 6 to give the corresponding dithiols with para-, meta- and ortho-location of the thiol groups, respectively. Domino-reaction of perfluoroindane-5-thiol and its acetyl thioester affords hexadecafluoro-2,12-dithia-pentacyclo[11.7.0.03,11.05,9.015,19]icosa-1(13),3,5(9),10,14,19-hexaene" @default.
- W4387298035 created "2023-10-04" @default.
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- W4387298035 date "2023-09-01" @default.
- W4387298035 modified "2023-10-04" @default.
- W4387298035 title "One-pot synthesis of perfluorinated benzenedithiols from perfluoroarenes and thioacetic acid" @default.
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- W4387298035 doi "https://doi.org/10.1016/j.mencom.2023.09.041" @default.
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