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- W2095536360 abstract "Reaction of o-Halobenzyl Cyanides with Carbon Disulfide and Phenyl Isothiocyanate Starting from o-halobenzyl cyanides 1 and carbon disulfide in the presence of sodium hydride dithiolates 3 are prepared, which are not isolated. Alkylation under cooling gives ketene S, S-acetals 4, while on heating at 100°C benzo[b]thiophenes 6 are obtained. Nitrile cyclisation yields thieno[2, 3-b]benzothiophene 7. Reaction of 1 with phenyl isothiocyanate/sodium hydride and subsequent alkylation leads to the ketene S, N-acetals 13 und to the thiazolidines 15." @default.
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- W2095536360 date "1979-01-01" @default.
- W2095536360 modified "2023-10-14" @default.
- W2095536360 title "Zur Reaktion von o-Halogenbenzylcyaniden mit Schwefelkohlenstoff und Phenylisothiocyanat" @default.
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- W2095536360 doi "https://doi.org/10.1002/prac.19793210618" @default.
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