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Aliphatic sulfonation. 3. Reactions of adamantylidenealkanes and cyclopropylidenealkanes with sulfur trioxide

✍ Scribed by Bakker, Bert H.; Cerfontain, Hans; Tomassen, Henk P. M.


Book ID
125849096
Publisher
American Chemical Society
Year
1989
Tongue
English
Weight
563 KB
Volume
54
Category
Article
ISSN
0022-3263

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πŸ“œ SIMILAR VOLUMES


Reactions of alkenoic acids with sulfur
✍ Ruud M. Schonk; B. H. Bakker; H. Cerfontain πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 English βš– 882 KB

## Abstract The reactions of the alkenoic acid derivatives 1a–19a with sulfur trioxide were studied in the temperature range βˆ’60 to 25Β°C using dichloromethane as solvent and 1.5 equiv. of dioxane as reactivity moderator. The alkenoic acids 13a and 14a, having a ‐(CH~2~)~4~‐ and ‐(CH~2~)~7~‐ linkage

Reactions of Ο‰-phenylalkenes with sulfur
✍ Ruud M. Schonk; Bert H. Bakker; Hans Cerfontain πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 English βš– 1018 KB

## Abstract Reactions of ω‐phenylalkenes 1a‐31a with sulfur trioxide were studied in the temperature range βˆ’60 to 25Β°C using dichloromethane as solvent and 1.5 mol equiv. of dioxane as reactivity moderator. ω‐Phenylalkenes 1a‐7a react just like simple alkenes: at low temperature, they yield the (th

Reactions of methylenecycloalkanes and c
✍ Ruud M. Schonk; Carel W. Meijer; Bert H. Bakker; Hans Cerfontain; Stephan ZΓΆllne πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 English βš– 543 KB

## Abstract Reactions of methylenecycloalkanes 1a‐4a and cycloalkylidenecycloalkanes 11a–14a with sulfur trioxide were studied in the temperature range βˆ’60 to 25Β°C using dichloromethane as solvent and 1.5 mol equiv. of dioxane relative to the amount of SO~3~ as reactivity moderator. Methylenecycloo