Mechanism and stereochemical considerations in the reaction of some arylserine derivatives with thionyl chloride
โ Scribed by Pines, Seemon H.; Kozlowski, Matthew A.; Karady, Sandor
- Book ID
- 121862292
- Publisher
- American Chemical Society
- Year
- 1969
- Tongue
- English
- Weight
- 767 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-3263
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Maahs and Hegenberg in their review of the chemistry of squaric acid (I) state: "Das Slure-dichlorid der QuadratsWure, Dichlor-cyclobutendion, lllsst sich aus Quadratsgure nicht herstellen." (1) Since dichlorocyclobutenedione (II) (2) is an important intermediate in the preparation of mono-and diary
Acetic acid thionyl chloride reaction was studied in chloro-, bromo-and nitrobenzene. The reaction seems to follow simple course in the beginning, but after some time complications occur. The percentage of hydrogen chloride in the effluent gases was determined by dissolving the gases in water and me