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- W2322685655 abstract "Aus entsprechenden Mercaptoacroleinen (II), die aus den Chlorderivaten (I) m 1 Mol Na-sulfid erhältlich sind, werden durch Umsetzung mit entsprechenden Chlorcrotonaldehyden (III) direkt die Thiopyrane (IV) erhalten; der Mercapto aldehyd (II) (R1 , R2: Phenyl) reagiert dagegen mit den Aldehyden (V) nur zu den Thioäthern (VI), die dann mit NaOH zu den Thiopyranen (VII) cyclisiert werden." @default.
- W2322685655 created "2016-06-24" @default.
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- W2322685655 date "1973-01-02" @default.
- W2322685655 modified "2023-10-17" @default.
- W2322685655 title "ChemInform Abstract: RK. VON BETA-CHLORVINYLALDEHYDEN 2. MITT. SYNTH. VON 2-FORMYLMETHYLEN-2H-THIOPYRANEN UND VORSTUFEN AUS BETA-CHLORVINYLALDEHYDEN" @default.
- W2322685655 cites W1607175185 @default.
- W2322685655 doi "https://doi.org/10.1002/chin.197301294" @default.
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