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- W2952336145 abstract "Primary, secondary, tertiary, allylic, and benzylic halides are converted efficiently into symmetric disulfides in high yields using thiourea as the sulfur atom source. The reactions are odorless and are performed at 30–35 °C in wet PEG-200 using MnO2 as an oxidant." @default.
- W2952336145 created "2019-06-27" @default.
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- W2952336145 date "2010-01-01" @default.
- W2952336145 modified "2023-09-25" @default.
- W2952336145 title "A one-pot, efficient, and odorless synthesis of symmetrical disulfides using organic halides and thiourea in the presence of manganese dioxide and wet polyethylene glycol (PEG-200)" @default.
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- W2952336145 doi "https://doi.org/10.1016/j.tetlet.2009.11.060" @default.
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