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- W2606363621 abstract "Das aus 2-Mercapto-äthanthiol und Acetanhydrid dargestellte Acetoxyäthanthiol (I) setzt sich mit dem Sulfenylchlorid (II) in Äther bei 0-5°C zu dem Disulfid (III) (100% Ausbeute) um, das durch Alkoholyse in Gegenwart von HCl das Hydrodisulfid (IV) (100%) liefert." @default.
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- W2606363621 date "1970-09-29" @default.
- W2606363621 modified "2023-09-25" @default.
- W2606363621 title "ChemInform Abstract: SYNTH. VON 2-SUBSTITUIERTEN AETHYLHYDRODISULFIDEN" @default.
- W2606363621 cites W1978721628 @default.
- W2606363621 doi "https://doi.org/10.1002/chin.197039202" @default.
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